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60 jobs found in north billerica, massachusetts

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    • cambridge, massachusetts
    • contract
    • $30 - $34.83 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $30.00 - 34.83 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support Drug Metabolism and Pharmacokinetics (DMPK) project representatives in coordinating discovery and development PK and PK/PD studies. Major responsibilities include: developing detailed study protocols to facilitate study coordination among multi-functional project team, operation group, and CROs. Tracking study progress to ensure study timeline are met.Format PK and PK/PD data, conduct initial analysis, and provide preliminary data interpretation.Collect the literature and scientific knowledge integration on biology, pharmacology, DMPK and clinical as needed.  qualifications: Bachelor or Master degree in Biology, Chemistry/Biochemistry, Pharmacology, Pharmaceutical Sciences, or related disciplinesHighly motivated and detail oriented with multi-tasking capabilities. Enthusiastic in learning drug discoveryExperience in pharmacokinetics, drug metabolism, pharmacodynamic and bioanalytical principles is preferredComfortable in working in multi-functional teams. Demonstrate strong inter-personal and problem solving skills.Strong oral and written communication capabilities. Proficient in Microsoft tools  skills: Pharmacology, MS-WORD, MS-EXCEL, Biology, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $30.00 - 34.83 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support Drug Metabolism and Pharmacokinetics (DMPK) project representatives in coordinating discovery and development PK and PK/PD studies. Major responsibilities include: developing detailed study protocols to facilitate study coordination among multi-functional project team, operation group, and CROs. Tracking study progress to ensure study timeline are met.Format PK and PK/PD data, conduct initial analysis, and provide preliminary data interpretation.Collect the literature and scientific knowledge integration on biology, pharmacology, DMPK and clinical as needed.  qualifications: Bachelor or Master degree in Biology, Chemistry/Biochemistry, Pharmacology, Pharmaceutical Sciences, or related disciplinesHighly motivated and detail oriented with multi-tasking capabilities. Enthusiastic in learning drug discoveryExperience in pharmacokinetics, drug metabolism, pharmacodynamic and bioanalytical principles is preferredComfortable in working in multi-functional teams. Demonstrate strong inter-personal and problem solving skills.Strong oral and written communication capabilities. Proficient in Microsoft tools  skills: Pharmacology, MS-WORD, MS-EXCEL, Biology, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lawrence, massachusetts
    • contract
    • $14.45 - $17 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lawrence, Massachusetts job type: Contract salary: $14.45 - 17.00 per hour work hours: 9 to 5 education: High School   responsibilities: Position Description: The Consumable tech will be responsible for manufacturing consumables according to SOP's , meeting company quality and efficiency standards. Position Requirements: - Work in consumable production with group lead or designated trainer - Possess basic manufacturing knowledge - Read, understand and execute SOP's - Basic computer skills - Additional duties as required or directed by the management team   qualifications: Qualifications: - Ability to stand for the duration of shift - Ability to lift 50 pounds - Good written and verbal communication skills - Attention to detail - ISO awareness Education High School Diploma or GED equivalent   skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lawrence, Massachusetts job type: Contract salary: $14.45 - 17.00 per hour work hours: 9 to 5 education: High School   responsibilities: Position Description: The Consumable tech will be responsible for manufacturing consumables according to SOP's , meeting company quality and efficiency standards. Position Requirements: - Work in consumable production with group lead or designated trainer - Possess basic manufacturing knowledge - Read, understand and execute SOP's - Basic computer skills - Additional duties as required or directed by the management team   qualifications: Qualifications: - Ability to stand for the duration of shift - Ability to lift 50 pounds - Good written and verbal communication skills - Attention to detail - ISO awareness Education High School Diploma or GED equivalent   skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • contract
    • $25 - $30 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations. Testing may include but not limited to samples from drug substance and drug product, manufacturing, stability, raw materials and various protocol studies using test methods. The assays range from pH, enzyme concentration to more complex assays such as SDS silver Gels, PCR, DNA and enzyme activity. This position is expected to maintain operational and GMP readiness of the QC areas. In addition, this position will participate in more complex projects, Operational excellence initiatives and various quality systems. 65% of work: Testing execution35% of work: QC operations support which entails data review, data trending, OE/5S initiative, maintenance of equipment and reagents, reagent prep, lab house keeping, support for other QC groups if needed.  qualifications: Essential: Bachelors degree and minimum of 0-2 years related experienceDesired: GMP knowledge, work experience Knowledge: Limited use and/or application of basic principles, theories and concepts.Limited knowledge of industry practices and standards. Position requires critical thinking.Key Skills: MS Office, LIMS, SAP, Trackwise, EDMS, Compliance and strong science understandingSolve routine problems of limited scope and complexity following established policies and procedures. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations of data from which answers can be readily obtained. Builds stable working relationships internally.The following physical abilities are required in order to fulfill the job duties:Repetitive bendings and reaching to setup and break down equipmentAbility to work around chemicalsAbility to wear personal protective equipment such as gloves, gowning, and respiratory protection in some casesAbility to walk and stand for periods of time Individual may be required to participate in environment chamber monitoring program which would include the use of an on- call mobile phone as well as on site support during non-business hours  skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Primary duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations. Testing may include but not limited to samples from drug substance and drug product, manufacturing, stability, raw materials and various protocol studies using test methods. The assays range from pH, enzyme concentration to more complex assays such as SDS silver Gels, PCR, DNA and enzyme activity. This position is expected to maintain operational and GMP readiness of the QC areas. In addition, this position will participate in more complex projects, Operational excellence initiatives and various quality systems. 65% of work: Testing execution35% of work: QC operations support which entails data review, data trending, OE/5S initiative, maintenance of equipment and reagents, reagent prep, lab house keeping, support for other QC groups if needed.  qualifications: Essential: Bachelors degree and minimum of 0-2 years related experienceDesired: GMP knowledge, work experience Knowledge: Limited use and/or application of basic principles, theories and concepts.Limited knowledge of industry practices and standards. Position requires critical thinking.Key Skills: MS Office, LIMS, SAP, Trackwise, EDMS, Compliance and strong science understandingSolve routine problems of limited scope and complexity following established policies and procedures. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations of data from which answers can be readily obtained. Builds stable working relationships internally.The following physical abilities are required in order to fulfill the job duties:Repetitive bendings and reaching to setup and break down equipmentAbility to work around chemicalsAbility to wear personal protective equipment such as gloves, gowning, and respiratory protection in some casesAbility to walk and stand for periods of time Individual may be required to participate in environment chamber monitoring program which would include the use of an on- call mobile phone as well as on site support during non-business hours  skills: Quality control, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $40 - $45.68 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $40.00 - 45.68 per hour work hours: 9 to 5 education: Bachelors   responsibilities: We are looking for an experienced individual with a strong background in histology to join our dynamic team of histotechnologists and pathologists as part of nonclinical safety assessment of new drug candidates. Perform basic histology procedures (e.g. handling unfixed and fixed human and animal tissues, accurate slide and cassette labeling, tissue trimming, processing, embedding, paraffin and frozen microtomy, routine H&E staining and special histochemical staining, coverslipping, archiving of specimens)Ensure and maintain preanalytical specimen handling integrity and quality to meet molecular pathology laboratory standards.Maintain adequate stock and efficient use of supplies necessary for performing all procedures, and preparation of reagents as required.Maintain laboratory equipment and assist with identification and execution of process improvement.Perform routine scanning of stained slides using slide image acquisition systems (e.g. Aperio ScanScope/Versa; Phillips Ultra Fast Scanner, or similar) and, manage the slide image database (e.g. Aperio eSlide manager; Phillips Philips IntelliSite Solution, or similar).Adhere to chemical agent, facility, and bio-facility safety requirements.Understand and follow Standard Operating Procedures (SOPs) and Study Protocol requirements for all laboratory assigned activities.Maintain proper documentation, archiving and routine quality control on all generated specimens and data in compliance with corporate policies and practices.Demonstrate a clear interest and ability in learning new skills along with the ability to be organized, multitask, communicate effectively with a team and diverse individuals.  qualifications: Minimum BS or MS degree in a Biological or Life Science.2-4+ years of relevant clinical or research histotechnology laboratory experience.The ideal candidate will have extensive experience with histology.Familiarity with immunohistochemistry, in situ hybridization, with the ability to independently troubleshoot and solve technical problems are desirable.Successful candidates will be able to work within a matrixed organization, across multiple reporting lines and functional areas.The position is within a laboratory in an expansion phase, with expectations for excellent interpersonal skills supporting and maintaining the current highly collaborative environment.Demonstrated strong background in IHC/ISH techniques, ASCP qualification in immunohistochemistry (QIHC) preferred.Necropsy experience is desirable.American Society for Clinical Pathology (ASCP) certification: HT (desirable), HTL (preferred).Experience with collection and documentation of research data in compliance with Good Laboratory Practices (GLPs) is desirable.  skills: SOP, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $40.00 - 45.68 per hour work hours: 9 to 5 education: Bachelors   responsibilities: We are looking for an experienced individual with a strong background in histology to join our dynamic team of histotechnologists and pathologists as part of nonclinical safety assessment of new drug candidates. Perform basic histology procedures (e.g. handling unfixed and fixed human and animal tissues, accurate slide and cassette labeling, tissue trimming, processing, embedding, paraffin and frozen microtomy, routine H&E staining and special histochemical staining, coverslipping, archiving of specimens)Ensure and maintain preanalytical specimen handling integrity and quality to meet molecular pathology laboratory standards.Maintain adequate stock and efficient use of supplies necessary for performing all procedures, and preparation of reagents as required.Maintain laboratory equipment and assist with identification and execution of process improvement.Perform routine scanning of stained slides using slide image acquisition systems (e.g. Aperio ScanScope/Versa; Phillips Ultra Fast Scanner, or similar) and, manage the slide image database (e.g. Aperio eSlide manager; Phillips Philips IntelliSite Solution, or similar).Adhere to chemical agent, facility, and bio-facility safety requirements.Understand and follow Standard Operating Procedures (SOPs) and Study Protocol requirements for all laboratory assigned activities.Maintain proper documentation, archiving and routine quality control on all generated specimens and data in compliance with corporate policies and practices.Demonstrate a clear interest and ability in learning new skills along with the ability to be organized, multitask, communicate effectively with a team and diverse individuals.  qualifications: Minimum BS or MS degree in a Biological or Life Science.2-4+ years of relevant clinical or research histotechnology laboratory experience.The ideal candidate will have extensive experience with histology.Familiarity with immunohistochemistry, in situ hybridization, with the ability to independently troubleshoot and solve technical problems are desirable.Successful candidates will be able to work within a matrixed organization, across multiple reporting lines and functional areas.The position is within a laboratory in an expansion phase, with expectations for excellent interpersonal skills supporting and maintaining the current highly collaborative environment.Demonstrated strong background in IHC/ISH techniques, ASCP qualification in immunohistochemistry (QIHC) preferred.Necropsy experience is desirable.American Society for Clinical Pathology (ASCP) certification: HT (desirable), HTL (preferred).Experience with collection and documentation of research data in compliance with Good Laboratory Practices (GLPs) is desirable.  skills: SOP, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $28.64 - $33.69 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $28.64 - 33.69 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Maintains and develops effective documentation systems appropriate for a research setting.Coordinates and ensures appropriate documentation for the Vaccine Research and Analytics laboratory.Facilitate and oversee the coordination, planning, assembly, writing, editing, and quality control of written research findings (reports, abstracts, manuscripts, systematic reviews, presentations, etc.) or regulatory documents (protocols, investigator brochures, study reports, etc.). Ensure data and reports are in compliance with regulatory standards, applicable SOPs, policies, procedures.Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content (exhibits, illustrations, tables, and appendices) for publication into finished documents appropriate for the stated audience. Participate in quality control review for documents written by other authors when requested.Write and review standard operating procedures (SOPs), laboratory procedures, equipment instructions, knowledge- based documents and business policies.Generate document templates and laboratory and equipment logs for general use.Manage templates and document versions in an electronic document management system (EDMS).Manage documents and training in a learning management system (LMS), to help plan, deliver and assess competencies.Develop an archiving plan and prepare records for archving in an electronic records management system (ERMS).Submit data and reports to Regulatory for inclusion in dossiers.Train technical staff and management in quality and documentation procedures, including good documentation practices, handling and review of electronic laboratory notebooks, data and reports.  qualifications: B.S degree in a scientific disciplineAt least 6 years laboratory experience, preferably in a clinical testing or analytical laboratory, Quality, or R&DMust have excellent written communication skills and attention to detail related to consistency, grammar, syntax, and accuracy.Must have experience working in a GXP environmentMust have experience writing and reviewing technical documentation, ideally have experience with advanced functions of Microsoft Word.Experience working in a GXP environment is preferred.Familiarity with regulatory processing and submissions is desirable.Experience with Electronic Document and Learning Management Systems is desirable.Experience working with and training cross functional groups. Must be creatively open to new ideas and methods and work with a spirit of continuous improvement and innovation.Ability to identify, report, and seek prompt corrections as they arise.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).  skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $28.64 - 33.69 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Maintains and develops effective documentation systems appropriate for a research setting.Coordinates and ensures appropriate documentation for the Vaccine Research and Analytics laboratory.Facilitate and oversee the coordination, planning, assembly, writing, editing, and quality control of written research findings (reports, abstracts, manuscripts, systematic reviews, presentations, etc.) or regulatory documents (protocols, investigator brochures, study reports, etc.). Ensure data and reports are in compliance with regulatory standards, applicable SOPs, policies, procedures.Work with authors/technical specialists to coordinate the completion of specialized content, to translate, write, edit and/or proof data and content (exhibits, illustrations, tables, and appendices) for publication into finished documents appropriate for the stated audience. Participate in quality control review for documents written by other authors when requested.Write and review standard operating procedures (SOPs), laboratory procedures, equipment instructions, knowledge- based documents and business policies.Generate document templates and laboratory and equipment logs for general use.Manage templates and document versions in an electronic document management system (EDMS).Manage documents and training in a learning management system (LMS), to help plan, deliver and assess competencies.Develop an archiving plan and prepare records for archving in an electronic records management system (ERMS).Submit data and reports to Regulatory for inclusion in dossiers.Train technical staff and management in quality and documentation procedures, including good documentation practices, handling and review of electronic laboratory notebooks, data and reports.  qualifications: B.S degree in a scientific disciplineAt least 6 years laboratory experience, preferably in a clinical testing or analytical laboratory, Quality, or R&DMust have excellent written communication skills and attention to detail related to consistency, grammar, syntax, and accuracy.Must have experience working in a GXP environmentMust have experience writing and reviewing technical documentation, ideally have experience with advanced functions of Microsoft Word.Experience working in a GXP environment is preferred.Familiarity with regulatory processing and submissions is desirable.Experience with Electronic Document and Learning Management Systems is desirable.Experience working with and training cross functional groups. Must be creatively open to new ideas and methods and work with a spirit of continuous improvement and innovation.Ability to identify, report, and seek prompt corrections as they arise.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).  skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • temporary
    • $28 - $30 per hour
    We are currently hiring for a QC Analyst at Takeda Pharmaceuticals, based in Lexington, MA.  This individual will support rhASA D/TAK-611 QC MV as a part of the QC HPLC team. This is a 9-month contract to start with the potential to extend from there.  Please reach out to ashley.cross@randstadusa.com with any questions!salary: $28 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesRole is responsible for HPLC laboratories performing a broad range of analytical based techniques such as SE-HPLC, RP-HPLC, IEX, CE-SDS, glycan and peptide analyses in order to support in-process, release and stability testing. Support commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation- introduction of new equipment and technology to improve sustainability and compliance is expected Provide support for Quality projects and implementation of operational excellence initiatives Areas of focus on techniques such as HPLC and SDS-PAGE for purity, identity, potency and charged heterogeneity. Perform and troubleshoot HPLC based assays (SE-HPLC, IEX, RP-HPLC, CE-SDS, Peptide Mapping, and Glycan Mapping) of release and stability Execute and lead method qualification and validation assays as needed Perform and lead OOT, OOS, GMP Investigations, data analysis, deviation and data trending Maintain GMP condition of the lab The essential functions of this role include:working in a smoke free environmentSkillsQuality ControlHPLCSDS-PAGEQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    We are currently hiring for a QC Analyst at Takeda Pharmaceuticals, based in Lexington, MA.  This individual will support rhASA D/TAK-611 QC MV as a part of the QC HPLC team. This is a 9-month contract to start with the potential to extend from there.  Please reach out to ashley.cross@randstadusa.com with any questions!salary: $28 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesRole is responsible for HPLC laboratories performing a broad range of analytical based techniques such as SE-HPLC, RP-HPLC, IEX, CE-SDS, glycan and peptide analyses in order to support in-process, release and stability testing. Support commercial and clinical testing for defined site-based and external programs, as well as method transfer and validation- introduction of new equipment and technology to improve sustainability and compliance is expected Provide support for Quality projects and implementation of operational excellence initiatives Areas of focus on techniques such as HPLC and SDS-PAGE for purity, identity, potency and charged heterogeneity. Perform and troubleshoot HPLC based assays (SE-HPLC, IEX, RP-HPLC, CE-SDS, Peptide Mapping, and Glycan Mapping) of release and stability Execute and lead method qualification and validation assays as needed Perform and lead OOT, OOS, GMP Investigations, data analysis, deviation and data trending Maintain GMP condition of the lab The essential functions of this role include:working in a smoke free environmentSkillsQuality ControlHPLCSDS-PAGEQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts (remote)
    • contract
    • $24.13 - $28.38 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $24.13 - 28.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Process import/export trade compliance clearance of cross-border shipments in Global Trade Management system (Oracle module)Maintenance of GTM systemsCommunication on shipments processing with different functions and customs brokersPre-validation and post audit of documentation related to customs clearancesVarious administrative support activities  qualifications: Experience with customs entry processes and data managementExperience preparing import licenses and permits with different government agencies (e.g. Customs, FDA, USDA, Aphis)Experience working with customs brokers. Background in entry writing and customs clearance is a plus.Experience with regulated industries (e.g. food, medical devices, pharma, etc.)Availability to work in US ET time zone, as well as early calls to coordinate with Europe locations.  skills: Import/Export Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $24.13 - 28.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Process import/export trade compliance clearance of cross-border shipments in Global Trade Management system (Oracle module)Maintenance of GTM systemsCommunication on shipments processing with different functions and customs brokersPre-validation and post audit of documentation related to customs clearancesVarious administrative support activities  qualifications: Experience with customs entry processes and data managementExperience preparing import licenses and permits with different government agencies (e.g. Customs, FDA, USDA, Aphis)Experience working with customs brokers. Background in entry writing and customs clearance is a plus.Experience with regulated industries (e.g. food, medical devices, pharma, etc.)Availability to work in US ET time zone, as well as early calls to coordinate with Europe locations.  skills: Import/Export Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • contract
    • $28 - $29 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Lexington, Massachusetts job type: Contract salary: $28 - 29 per hour work hours: 3 to 11 education: High School   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. · Execution of critical and routine activities in support of production · Perform Batch Record, Log Book and Form Prep requests · Enter data in the Laboratory Information Management System (LIMS) , MODA and or other business functions · Troubleshoot and resolve basic process related issues · Recognize and escalate deviation · Review GMP documentation · Sample preparation and testing · Identify changes needed to documentation · Participate in tiered visual management system and support CI initiatives · Complete required training on time · Initiate work orders · Assemble and disassemble process equipment · Perform scheduled cleaning of equipment · Perform standardization of equipment · Support change over activities · Execution of equipment and process qualifications as well as validation   qualifications: · Takes the initiative to openly express ideas and concerns · Establishes credibility and acts responsibly to earn the confidence, trust and respect of others · Recognizes and acknowledges others' contributions to team success · Proactively assists others in accomplishing work · Builds and maintains productive relationships based on mutual trust and respect · Professionally communicates with all business partners · Establishes challenging goals and holds self-accountable for achieving them · Effectively manages multiple assignments and competing priorities by maximizing time, being well organized and utilizing available resources · Ensures delivery of accurate and complete work within designated timelines · Understands and follows the Code of Conduct, policies, and procedures relevant to job accountabilities · Effectively demonstrates an understanding of the company's core business in meeting the needs of others · Demonstrates ability to solve problems by analyzing issues and making informed recommendations · Adjusts work by organizing and prioritizing tasks in the face of changing business needs. · Demonstrates a professional approach in adapting to change · Adapts work products, processes and services in response to changes in the business environment · Listens carefully and is receptive to feedback from others · Demonstrates a willingness to admit one's mistakes and modify approach to ensure a positive outcome · Demonstrates composure under trying circumstances and approaches problems professionally · Actively seeks opportunities for personal growth and development and monitors progress toward achieving development goals · Consistently utilizes available resources to acquire, develop and apply new skills and knowledge · Responds to feedback by capitalizing on strengths and building upon areas of improvement for the benefit of the organization   skills: SOP, Laboratory Information Management Systems (LIMS), ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Lexington, Massachusetts job type: Contract salary: $28 - 29 per hour work hours: 3 to 11 education: High School   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. · Execution of critical and routine activities in support of production · Perform Batch Record, Log Book and Form Prep requests · Enter data in the Laboratory Information Management System (LIMS) , MODA and or other business functions · Troubleshoot and resolve basic process related issues · Recognize and escalate deviation · Review GMP documentation · Sample preparation and testing · Identify changes needed to documentation · Participate in tiered visual management system and support CI initiatives · Complete required training on time · Initiate work orders · Assemble and disassemble process equipment · Perform scheduled cleaning of equipment · Perform standardization of equipment · Support change over activities · Execution of equipment and process qualifications as well as validation   qualifications: · Takes the initiative to openly express ideas and concerns · Establishes credibility and acts responsibly to earn the confidence, trust and respect of others · Recognizes and acknowledges others' contributions to team success · Proactively assists others in accomplishing work · Builds and maintains productive relationships based on mutual trust and respect · Professionally communicates with all business partners · Establishes challenging goals and holds self-accountable for achieving them · Effectively manages multiple assignments and competing priorities by maximizing time, being well organized and utilizing available resources · Ensures delivery of accurate and complete work within designated timelines · Understands and follows the Code of Conduct, policies, and procedures relevant to job accountabilities · Effectively demonstrates an understanding of the company's core business in meeting the needs of others · Demonstrates ability to solve problems by analyzing issues and making informed recommendations · Adjusts work by organizing and prioritizing tasks in the face of changing business needs. · Demonstrates a professional approach in adapting to change · Adapts work products, processes and services in response to changes in the business environment · Listens carefully and is receptive to feedback from others · Demonstrates a willingness to admit one's mistakes and modify approach to ensure a positive outcome · Demonstrates composure under trying circumstances and approaches problems professionally · Actively seeks opportunities for personal growth and development and monitors progress toward achieving development goals · Consistently utilizes available resources to acquire, develop and apply new skills and knowledge · Responds to feedback by capitalizing on strengths and building upon areas of improvement for the benefit of the organization   skills: SOP, Laboratory Information Management Systems (LIMS), ICH Regulations, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • woburn, massachusetts
    • permanent
    • $60,000 - $70,000 per year
    job summary: Woburn MA based cryogenics research company who offers cryogenic systems for a broad range of applications, with cooling provided by liquid helium, liquid nitrogen or mechanical refrigerators is actively seeking (1) highly skilled Senior Laboratory Technician to start immediately within the next 2-3wks. Working hours will be hours are 6:45am - 3:15pm. The Lab Technician will be responsible for the hands-on assembly of Ultra-low temperature cryogenic products including dilution refrigerator system and He-3 cryostat. Ideal candidate should have knowledge of wiring, soldering, reading, and working from mechanical assembly drawings and/or solid work. Working with mass spectrometer leak detectors, vacuum pumps, low-temperature thermometers transferring cryogens and trouble-shooting cryogenic systems. Basic electrical and electronics knowledge. Good experience working with laboratory tools and facilities. This position requires good manual dexterity and working with small parts and fine wires. Great location off routes 93 and 95, also commuter rail access from Lowell and Boston. Plenty of great shopping spots, restaurants and a easy commute to tax-free New Hampshire!!   location: Woburn, Massachusetts job type: Permanent salary: $60,000 - 70,000 per year work hours: 7 to 3 education: Associate   responsibilities: Perform all functions of lab technicianPerform all phases of assembly with minimal supervision and ≥80% efficiency on the following systems: All models of He-3 cryostatAll models of dilution refrigerator systemsAll gas handling systems for continuous flow type cryostats Able to create a reliable vacuum seal, such as O-ring seal, indium seal, CF seal, etc.Able to charge and decontaminate a cryocooler/compressor systemAble to train other Lab TechniciansNo supervisory responsibilities for this position.Basic vacuum knowledgeFamiliar with vacuum greaseBeing able to do perform basic vacuum pump serviceSkillful for leak checkingKnowledge on epoxy Able to read and understand the epoxy matrixAble to use 5 minute, Stycast 2850, Araldite epoxy etc.Understand different function for different type of epoxies Knowledge on electricity Understand Ohm's law (V=IR) and powerProper use of DMMKnow difference between AC and DCAware of different wall socket voltages (120 VAC, 220 VAC, 380 VAC, and 480 VAC)Aware of two frequencies (60Hz, 50Hz) Aware of two phases of power (single, three)  qualifications: Minimum Experience: 2 yearsEducation Requirements: High School Diploma, Trade/Technical SchoolSufficient computer skills for the following:Read SW model or e-drawingRead BOM and search parts  skills: MS-WORD, MS-Project, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), Manufacturing Operations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Woburn MA based cryogenics research company who offers cryogenic systems for a broad range of applications, with cooling provided by liquid helium, liquid nitrogen or mechanical refrigerators is actively seeking (1) highly skilled Senior Laboratory Technician to start immediately within the next 2-3wks. Working hours will be hours are 6:45am - 3:15pm. The Lab Technician will be responsible for the hands-on assembly of Ultra-low temperature cryogenic products including dilution refrigerator system and He-3 cryostat. Ideal candidate should have knowledge of wiring, soldering, reading, and working from mechanical assembly drawings and/or solid work. Working with mass spectrometer leak detectors, vacuum pumps, low-temperature thermometers transferring cryogens and trouble-shooting cryogenic systems. Basic electrical and electronics knowledge. Good experience working with laboratory tools and facilities. This position requires good manual dexterity and working with small parts and fine wires. Great location off routes 93 and 95, also commuter rail access from Lowell and Boston. Plenty of great shopping spots, restaurants and a easy commute to tax-free New Hampshire!!   location: Woburn, Massachusetts job type: Permanent salary: $60,000 - 70,000 per year work hours: 7 to 3 education: Associate   responsibilities: Perform all functions of lab technicianPerform all phases of assembly with minimal supervision and ≥80% efficiency on the following systems: All models of He-3 cryostatAll models of dilution refrigerator systemsAll gas handling systems for continuous flow type cryostats Able to create a reliable vacuum seal, such as O-ring seal, indium seal, CF seal, etc.Able to charge and decontaminate a cryocooler/compressor systemAble to train other Lab TechniciansNo supervisory responsibilities for this position.Basic vacuum knowledgeFamiliar with vacuum greaseBeing able to do perform basic vacuum pump serviceSkillful for leak checkingKnowledge on epoxy Able to read and understand the epoxy matrixAble to use 5 minute, Stycast 2850, Araldite epoxy etc.Understand different function for different type of epoxies Knowledge on electricity Understand Ohm's law (V=IR) and powerProper use of DMMKnow difference between AC and DCAware of different wall socket voltages (120 VAC, 220 VAC, 380 VAC, and 480 VAC)Aware of two frequencies (60Hz, 50Hz) Aware of two phases of power (single, three)  qualifications: Minimum Experience: 2 yearsEducation Requirements: High School Diploma, Trade/Technical SchoolSufficient computer skills for the following:Read SW model or e-drawingRead BOM and search parts  skills: MS-WORD, MS-Project, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), Manufacturing Operations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts (remote)
    • contract
    • $75 - $90 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $75 - 90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This position will primarily be responsible for the following activities under the guidance of the Patient Engagement Disease Unit Leads and the Head of Program and Study Leadership: support programs and teams by developing a strategy for the recruitment and retention of patients- provide input to the study team by identifying key issues and barriers to successful recruitment and retention- including digital strategies and health equality needsSupport study teams regarding the assessment/ incorporation of patient and/or caregiver input into Company protocols to influence study design with the goal of generating data to support executable, patient friendly study designs and assessments.Include recruitment strategies to support underserved/underrepresented populations access to clinical trialsIntegrate Patient Engagement efforts with other key groups eg Company Patient AdvocacyAlong with our CRO provide vendor oversight of recruitment and retention vendorsRole will include maintaining trackers and metrics to regarding ROI of recruitment tactics.Role will liaise with other groups outside GCO such as R&D business operations, procurement, sourcing, finance, Legal as needed.   qualifications: Approximately 8 years of clinical research / project management experience in the sponsor or CRO setting.Must have at least 2 years' experience of working in a similar Patient Engagement role in Clinical Trials.Risk management, mitigation and problem-solvingFamiliarity with GCPProven ability to multi-task and thrive in a fast-paced environmentWorks and meets deadlines while being detailed orientedSelf-motivatorDedication to quality in all work tasks and deliverablesAbility to work effectively in cross-functional and global teams  skills: MS-WORD, MS-EXCEL, GCP (Good Clinical Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $75 - 90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This position will primarily be responsible for the following activities under the guidance of the Patient Engagement Disease Unit Leads and the Head of Program and Study Leadership: support programs and teams by developing a strategy for the recruitment and retention of patients- provide input to the study team by identifying key issues and barriers to successful recruitment and retention- including digital strategies and health equality needsSupport study teams regarding the assessment/ incorporation of patient and/or caregiver input into Company protocols to influence study design with the goal of generating data to support executable, patient friendly study designs and assessments.Include recruitment strategies to support underserved/underrepresented populations access to clinical trialsIntegrate Patient Engagement efforts with other key groups eg Company Patient AdvocacyAlong with our CRO provide vendor oversight of recruitment and retention vendorsRole will include maintaining trackers and metrics to regarding ROI of recruitment tactics.Role will liaise with other groups outside GCO such as R&D business operations, procurement, sourcing, finance, Legal as needed.   qualifications: Approximately 8 years of clinical research / project management experience in the sponsor or CRO setting.Must have at least 2 years' experience of working in a similar Patient Engagement role in Clinical Trials.Risk management, mitigation and problem-solvingFamiliarity with GCPProven ability to multi-task and thrive in a fast-paced environmentWorks and meets deadlines while being detailed orientedSelf-motivatorDedication to quality in all work tasks and deliverablesAbility to work effectively in cross-functional and global teams  skills: MS-WORD, MS-EXCEL, GCP (Good Clinical Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $83.42 - $98.14 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $83.42 - 98.14 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing a Core Dossier for Module 3 and preparing Module 3 documents to support Marketing Authorization Applications in Japan and Brazil. Provide support to other HA interactions as required. Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC and manufacturing teams to ensure that all applicable regulatory requirements are considered and appropriately incorporated into submissions for marketing authorizations.Provide Reg CMC support for development programs to ensure that products are developed and manufactured in compliance with appropriate regulations and guidelines so that they be studied and marketed as planned.Manage preparation of Core Dossier, Japan and Brazil applications in a timely manner to meet corporate objectives. Collaborate with EU & International regulatory colleagues to ensure global perspective and provide support in the preparation of EU and International regulatory documentation in a timely manner to meet corporate objectives. 30%: Develop global CMC Core Dossier for Module 3 20%: Prepare Module 3 Marketing Authorization Application for Japan 30%: Prepare Module 3 Marketing Authorization Application for Brazil. 10%: Review and approve technical documentation including technology transfer protocols, validation protocols, technical reports, manufacturing and labeling information to assure conformance with regulations; and regulatory guidelines. 10%: Provide CMC regulatory guidance to project / product teams.   qualifications: B.A. / B.A./ M.S. / Ph.D. in biochemistry, chemistry, biology or related pharmaceutical field. Minimum of 4 years experience in pharmaceutical product development including significant experience in CMC regulatory affairs with a strong biologics background or equivalent.Experience in directing interactions with regulatory authorities desired.Knowledgeable in ICH and FDA guidelines relevant to CMC aspects of product development and maintenance. Significant coordination with cross-functional teams internally and regulatory authorities externally.   skills: CMC, FDA, GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Submissions, ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $83.42 - 98.14 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing a Core Dossier for Module 3 and preparing Module 3 documents to support Marketing Authorization Applications in Japan and Brazil. Provide support to other HA interactions as required. Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC and manufacturing teams to ensure that all applicable regulatory requirements are considered and appropriately incorporated into submissions for marketing authorizations.Provide Reg CMC support for development programs to ensure that products are developed and manufactured in compliance with appropriate regulations and guidelines so that they be studied and marketed as planned.Manage preparation of Core Dossier, Japan and Brazil applications in a timely manner to meet corporate objectives. Collaborate with EU & International regulatory colleagues to ensure global perspective and provide support in the preparation of EU and International regulatory documentation in a timely manner to meet corporate objectives. 30%: Develop global CMC Core Dossier for Module 3 20%: Prepare Module 3 Marketing Authorization Application for Japan 30%: Prepare Module 3 Marketing Authorization Application for Brazil. 10%: Review and approve technical documentation including technology transfer protocols, validation protocols, technical reports, manufacturing and labeling information to assure conformance with regulations; and regulatory guidelines. 10%: Provide CMC regulatory guidance to project / product teams.   qualifications: B.A. / B.A./ M.S. / Ph.D. in biochemistry, chemistry, biology or related pharmaceutical field. Minimum of 4 years experience in pharmaceutical product development including significant experience in CMC regulatory affairs with a strong biologics background or equivalent.Experience in directing interactions with regulatory authorities desired.Knowledgeable in ICH and FDA guidelines relevant to CMC aspects of product development and maintenance. Significant coordination with cross-functional teams internally and regulatory authorities externally.   skills: CMC, FDA, GCP (Good Clinical Practice), Regulatory Affairs Operations, Regulatory Affairs Strategy, Submissions, ICH Regulations Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • contract
    • $80.20 - $94.35 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $80.20 - 94.35 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Materials & Process Scientist for the Raw Material Alternatives Taskforce will act as a technical SME and facilitator to develop a consistent approach for the global implementation of alternative suppliers of raw materials used in manufacturing. He/she will be responsible for developing technical plans to evaluate alternate materials, translating supply mitigation strategies into executable implementation work plans, and partnering with personnel at manufacturing sites to understand and evaluate site-specific material requirements. He/She will be the liaison between Technical process experts (Global manufacturing sciences, local manufacturing sciences, and material qualification) as well as the manufacturing and Quality organizations to ensure implementation progression and uninterrupted manufacturing. This individual will provide global value by centralizing of non-product- and non-site-specific tasks. This is an individual contributor role with cross-functional leadership responsibilities. Compare current and proposed new raw materials, and identify differences and risks to product quality, process performance, and patient safetyCollaborate cross functionally to define technical requirements and activities needed to implement alternative raw materials based on category of material.Standardize the implementation approach of alternatives across multiple manufacturing sites and impacted products.Translate supply risks and mitigation proposals into executable tasks and implementation plans at manufacturing site level.Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  qualifications: Required BS in engineering, life sciences, or related field with a minimum 10 years' experience, MS with a minimum of 8 years' experience, or PhD with 2-5 years' experience in pharmaceutical development and manufacturing (preferred), or experience in medical devices or other adjacent industriesExperience working in a GMP environmentStrong project leadership/project management experience with a successful track record of change management projects and processes.Strong communication and interpersonal skills.Ability to collaborate and work cross-functionally in a global environment. Preferred Expertise in one or more of the following: single use systems, filters, chromatography resins, chemicals, cell culture media, excipients, elemental impurities analysis, extractable and leachables assessments, dual sourcing of raw materials.Working knowledge of GMP biologics manufacturing processes and a comprehensive understanding of dependencies between materials, processes, and final product.High level of professionalism and business etiquette when communicating with cross-functional teams, and external suppliers.Ability to manage numerous priorities simultaneouslyLead projects and meetings effectively.Ability to influence and interact well with others (customers, peers and others in more senior positions)Proficient in the use of Microsoft Office including Word, Excel, Visio, and Power PointApply industry guidelines and applicable technology standards to decision making processesProvides leadership on cross-functional teamsProvides leadership to drive highly complex projects including ones that span multiple sites and productsConsult and collaborate with cross-functional teams including but not limited to Global Process Sciences, local Manufacturing Sciences, Material Qualification, Quality, Manufacturing, Engineering, Procurement & Supply chain.Act as a representative in cross-functional teams, leading the global implementation of alternative suppliers of raw materials used in manufacturing. Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Chromatography, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lexington, Massachusetts job type: Contract salary: $80.20 - 94.35 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Materials & Process Scientist for the Raw Material Alternatives Taskforce will act as a technical SME and facilitator to develop a consistent approach for the global implementation of alternative suppliers of raw materials used in manufacturing. He/she will be responsible for developing technical plans to evaluate alternate materials, translating supply mitigation strategies into executable implementation work plans, and partnering with personnel at manufacturing sites to understand and evaluate site-specific material requirements. He/She will be the liaison between Technical process experts (Global manufacturing sciences, local manufacturing sciences, and material qualification) as well as the manufacturing and Quality organizations to ensure implementation progression and uninterrupted manufacturing. This individual will provide global value by centralizing of non-product- and non-site-specific tasks. This is an individual contributor role with cross-functional leadership responsibilities. Compare current and proposed new raw materials, and identify differences and risks to product quality, process performance, and patient safetyCollaborate cross functionally to define technical requirements and activities needed to implement alternative raw materials based on category of material.Standardize the implementation approach of alternatives across multiple manufacturing sites and impacted products.Translate supply risks and mitigation proposals into executable tasks and implementation plans at manufacturing site level.Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  qualifications: Required BS in engineering, life sciences, or related field with a minimum 10 years' experience, MS with a minimum of 8 years' experience, or PhD with 2-5 years' experience in pharmaceutical development and manufacturing (preferred), or experience in medical devices or other adjacent industriesExperience working in a GMP environmentStrong project leadership/project management experience with a successful track record of change management projects and processes.Strong communication and interpersonal skills.Ability to collaborate and work cross-functionally in a global environment. Preferred Expertise in one or more of the following: single use systems, filters, chromatography resins, chemicals, cell culture media, excipients, elemental impurities analysis, extractable and leachables assessments, dual sourcing of raw materials.Working knowledge of GMP biologics manufacturing processes and a comprehensive understanding of dependencies between materials, processes, and final product.High level of professionalism and business etiquette when communicating with cross-functional teams, and external suppliers.Ability to manage numerous priorities simultaneouslyLead projects and meetings effectively.Ability to influence and interact well with others (customers, peers and others in more senior positions)Proficient in the use of Microsoft Office including Word, Excel, Visio, and Power PointApply industry guidelines and applicable technology standards to decision making processesProvides leadership on cross-functional teamsProvides leadership to drive highly complex projects including ones that span multiple sites and productsConsult and collaborate with cross-functional teams including but not limited to Global Process Sciences, local Manufacturing Sciences, Material Qualification, Quality, Manufacturing, Engineering, Procurement & Supply chain.Act as a representative in cross-functional teams, leading the global implementation of alternative suppliers of raw materials used in manufacturing. Serve as the communication pathway between CMC teams and Local sites to project governance for reporting project progress, risks, and issues.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Chromatography, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $30 - $34.60 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $30.00 - 34.60 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The company is seeking a highly motivated biologist to join the Bioassays & HTS team in support of Gene Therapy projects within the Biotherapeutic & Medicinal Sciences department. Our group develops small format assays, executes high throughput screens (HTS) and the subsequent assessment of candidate molecules as part of a collaborative team of scientists. The primary responsibilities for this position are development and implementation of innovative cell-based assays using high throughput technologies, use of data analysis tools to assess biological activity and advance portfolio projects. The candidate must have experience with in vitro cell culture, use of primary cells plus experience with a preference for experience in neurobiology. The successful candidate will accomplish our mission through innovation, open communication, teamwork, creative problem solving, and the use of state-of-the-art technologies. In collaboration with the Gene Therapy Acceleration Unit (GTx), we aim to develop and implement assays to study various aspects of gene therapy and therapeutic candidates in vitro. This individual will contribute to key projects through the application of mammalian cell culture, semi-automated liquid handling, data handling and data analysis. Additional responsibilities include robust documentation of experiments in an electronic notebook, working with assay scientists and automation engineers to increase instrument performance, and execute screens through the use of cell types relevant to neurology. The candidate is expected to design scientific experiments and perform comprehensive data analysis using specialized software to process HTS and dose response data (e.g. TIBCO Spotfire, Genedata Screener).   qualifications: Legal authorization to work in the U.S.This position requires a Bachelor's degree in Biology or a related discipline and experience with HTS instruments to support drug discoveryDemonstrated broad expertise in various assay methodologies including high content analysis (confocal microscopy), standard plate reader compatible assays including protein-protein interaction readouts (e.g. FRET/BRET, AlphaLISA, MSD).Familiarity with Hamilton and Biomek workstations, Labcyte Echo, HighRes systems and various fluid handlers is preferredThe successful candidate will be highly motivated with a demonstrated ability to successfully take on challenges, troubleshoot efficiently and quickly adapt to new responsibilitiesThe candidate must have excellent organization, oral and written communication skillsThe ability to collaborate and work effectively as part of a team is essential  skills: Assay Development, In Vitro, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $30.00 - 34.60 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The company is seeking a highly motivated biologist to join the Bioassays & HTS team in support of Gene Therapy projects within the Biotherapeutic & Medicinal Sciences department. Our group develops small format assays, executes high throughput screens (HTS) and the subsequent assessment of candidate molecules as part of a collaborative team of scientists. The primary responsibilities for this position are development and implementation of innovative cell-based assays using high throughput technologies, use of data analysis tools to assess biological activity and advance portfolio projects. The candidate must have experience with in vitro cell culture, use of primary cells plus experience with a preference for experience in neurobiology. The successful candidate will accomplish our mission through innovation, open communication, teamwork, creative problem solving, and the use of state-of-the-art technologies. In collaboration with the Gene Therapy Acceleration Unit (GTx), we aim to develop and implement assays to study various aspects of gene therapy and therapeutic candidates in vitro. This individual will contribute to key projects through the application of mammalian cell culture, semi-automated liquid handling, data handling and data analysis. Additional responsibilities include robust documentation of experiments in an electronic notebook, working with assay scientists and automation engineers to increase instrument performance, and execute screens through the use of cell types relevant to neurology. The candidate is expected to design scientific experiments and perform comprehensive data analysis using specialized software to process HTS and dose response data (e.g. TIBCO Spotfire, Genedata Screener).   qualifications: Legal authorization to work in the U.S.This position requires a Bachelor's degree in Biology or a related discipline and experience with HTS instruments to support drug discoveryDemonstrated broad expertise in various assay methodologies including high content analysis (confocal microscopy), standard plate reader compatible assays including protein-protein interaction readouts (e.g. FRET/BRET, AlphaLISA, MSD).Familiarity with Hamilton and Biomek workstations, Labcyte Echo, HighRes systems and various fluid handlers is preferredThe successful candidate will be highly motivated with a demonstrated ability to successfully take on challenges, troubleshoot efficiently and quickly adapt to new responsibilitiesThe candidate must have excellent organization, oral and written communication skillsThe ability to collaborate and work effectively as part of a team is essential  skills: Assay Development, In Vitro, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $52,000 - $78,000 per year
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment.   location: North Billerica, Massachusetts job type: Permanent salary: $52,000 - 78,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: The Quality Management System Technical Specialist supports the company's Quality Systems processes, both paper and within the electronic Quality Management System. This individual supports the maintenance and enhancement of existing processes (change control, quality events, controlled documentation, records management, training, and others) and the implementation of new systems and processes. Support the electronic Quality Management System (CATSWeb QMS) and its users as a business-level superuser / administrator. Train users / develop training material, help users find information in the system, trouble-shoot process issues, and participate in implementation of updates and enhancements to Quality Systems processes; including change control, CAPA, deviations, complaints, document management, and training.Propose and implement improvements to Quality Systems business processes, to increase efficiency, enhance compliance and reduce system maintenance requirements.Provide project and validation support for all activities involving modifications, upgrades and or business process changes related to Quality Systems applications. Author validation documentation and execute validation activities in accordance with company and industry standards.Participate in the design and implementation of new or updated processes. Collaborate with end users to document user and functional requirements for new implementations or upgrades to processes and systems. May act as a business lead for small to medium size projects.Partner with the IT organization and vendors to resolve issues and manage initiatives related to the Quality Management System.Work as a team player across many functions, departments, and groups, acting as a technical / quality management system resource.Support regulatory agency inspections as a Subject Matter Expert and by participating in back room processes, such as information retrieval.Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards.Actively demonstrates the company values.  qualifications: BS/BA degree in a scientific or technical field, with a minimum of 5 years experience in a GxP environment.Experience with electronic Quality Management Systems at the technical support level is highly desirable. Experience with the support of CATSWeb QMS is a plus.A combination of education, training and experience may be considered in lieu of the above stated qualifications.Must have excellent written, verbal, and presentation skills. Must be able to interact effectively with all levels of management.Excellent organizational, analytical, and problem-solving skills and strong attention to detail.  skills: Quality Assurance, CAPA Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment.   location: North Billerica, Massachusetts job type: Permanent salary: $52,000 - 78,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: The Quality Management System Technical Specialist supports the company's Quality Systems processes, both paper and within the electronic Quality Management System. This individual supports the maintenance and enhancement of existing processes (change control, quality events, controlled documentation, records management, training, and others) and the implementation of new systems and processes. Support the electronic Quality Management System (CATSWeb QMS) and its users as a business-level superuser / administrator. Train users / develop training material, help users find information in the system, trouble-shoot process issues, and participate in implementation of updates and enhancements to Quality Systems processes; including change control, CAPA, deviations, complaints, document management, and training.Propose and implement improvements to Quality Systems business processes, to increase efficiency, enhance compliance and reduce system maintenance requirements.Provide project and validation support for all activities involving modifications, upgrades and or business process changes related to Quality Systems applications. Author validation documentation and execute validation activities in accordance with company and industry standards.Participate in the design and implementation of new or updated processes. Collaborate with end users to document user and functional requirements for new implementations or upgrades to processes and systems. May act as a business lead for small to medium size projects.Partner with the IT organization and vendors to resolve issues and manage initiatives related to the Quality Management System.Work as a team player across many functions, departments, and groups, acting as a technical / quality management system resource.Support regulatory agency inspections as a Subject Matter Expert and by participating in back room processes, such as information retrieval.Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards.Actively demonstrates the company values.  qualifications: BS/BA degree in a scientific or technical field, with a minimum of 5 years experience in a GxP environment.Experience with electronic Quality Management Systems at the technical support level is highly desirable. Experience with the support of CATSWeb QMS is a plus.A combination of education, training and experience may be considered in lieu of the above stated qualifications.Must have excellent written, verbal, and presentation skills. Must be able to interact effectively with all levels of management.Excellent organizational, analytical, and problem-solving skills and strong attention to detail.  skills: Quality Assurance, CAPA Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • billerica, massachusetts
    • temporary
    • $23 - $25 per hour
    Global company seeking candidates with 1-2 years of experience working in a laboratory setting, with a background in Chemistry, Chemical Engineering, or Biology, or at least have a recent Associate or Bachelor Degree in one of those fields of study.  Schedule is 2PM - 11PM Monday to Friday On a typical day, you would: Come in at 2PM, go through requests, get samples to look at, talk about what instruments to use to look at those samples, interpret the data, and write a report. Other Duties: Lab Maintenance, Projects, Sample Analysissalary: $23 - $25 per hourshift: Secondwork hours: 2 PM - 11 PMeducation: AssociateResponsibilitiesThis role will be responsible for performing analysis to support membrane R&D and new liquid filtration and purification products development in the Micro-contamination Control (MC) Division of Entegris. The role will involve wet chemistry and operating several analytical techniques like ICP-MS, GCMS, LCMS, etc. The ideal candidate will be results oriented and an excellent team player, with knowledge of general lab instrument operations and safe handling/disposal of chemicals. In this role you will Execute laboratory testing according to standard operating procedures (SOPs), make observations and interpret findings Write technical reports and communicate testing status/results verbally and in writing. Drive for continuous improvement of existing testing method Maintain lab supplies, equipment, and instruments. Support senior level scientists on new method development and technical innovation. Continuous training on various analytical techniques and methods; The essential functions of this role include:working in a smoke free environmentSkillschemistryQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Global company seeking candidates with 1-2 years of experience working in a laboratory setting, with a background in Chemistry, Chemical Engineering, or Biology, or at least have a recent Associate or Bachelor Degree in one of those fields of study.  Schedule is 2PM - 11PM Monday to Friday On a typical day, you would: Come in at 2PM, go through requests, get samples to look at, talk about what instruments to use to look at those samples, interpret the data, and write a report. Other Duties: Lab Maintenance, Projects, Sample Analysissalary: $23 - $25 per hourshift: Secondwork hours: 2 PM - 11 PMeducation: AssociateResponsibilitiesThis role will be responsible for performing analysis to support membrane R&D and new liquid filtration and purification products development in the Micro-contamination Control (MC) Division of Entegris. The role will involve wet chemistry and operating several analytical techniques like ICP-MS, GCMS, LCMS, etc. The ideal candidate will be results oriented and an excellent team player, with knowledge of general lab instrument operations and safe handling/disposal of chemicals. In this role you will Execute laboratory testing according to standard operating procedures (SOPs), make observations and interpret findings Write technical reports and communicate testing status/results verbally and in writing. Drive for continuous improvement of existing testing method Maintain lab supplies, equipment, and instruments. Support senior level scientists on new method development and technical innovation. Continuous training on various analytical techniques and methods; The essential functions of this role include:working in a smoke free environmentSkillschemistryQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $48.68 - $57.27 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $48.68 - 57.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. Independently use appropriate experimental procedure to accomplish an assigned project or design and implement new methodologies to address specific research questions.Prepare technical reports, summaries, protocols, and quantitative analyses of experimental procedures, data, and conclusions. Author and/or edit lab procedures and quality records under Quality Assurance program.Communicates and/or presents results of own work, both oral and written results to supervisor, monthly/annual progress report meetings, and/or project teams. Participates in project planning strategy and overall project execution. May be responsible for a larger project area or multiple smaller projects.Routinely perform and participate in on-going experiments regarding the all assigned programs that also encompass independently designing new or modifying/optimizing current procedures and/or techniques as needed.Develop, design, and implement new procedures by researching and extracting information from scientific literature and/or collaborating or consulting with internal and external personnel to drive progress on research projects.Make detailed observations, record, organize, analyze data, and interpret results in a clear and logical format (e.g., graphs, charts, summaries, etc.). Make routine sound scientific conclusions and decisions within assigned programs; assemble and interpret own data for internal presentations.Recognizes inconsistencies and interprets experimental outcomes. Identify problems with experiments and troubleshoot solutions.Participate in technical transfer of protocols to outsourced companies, provide reagents, and act as troubleshooting contact to external company.Low degree of supervision required within assigned project area.May act as lead worker and be able to train or provide work directions for Research Associate I, II, and/or student interns.Independently implement methods using journal articles and/or other scientists as resources, with a medium degree of supervision.Write and maintain accurate, complete, and timely data in laboratory notebooks.mammalian cells required.Expertise working with virus infectivity assays preferred.Knowledge of theoretical basis and concepts of experimental design and how they fit into overall project goals.Maintain familiarity with current applicable scientific literature and contribute to the process of a project within her/his scientific discipline, as well as investigate, create, and develop new methods and techniques for project advancement.  qualifications: MS Degree in Physical or Life Sciences and 3 years laboratory experience, or BS Degree in Physical or Life Sciences and at least 5 years laboratory experience.Possess a combination of education and experience in a physical and/or life science to work independently, serve as a resource for researchers, train new technicians, and help solve problems with instrument operation.Personal motivation to expand applicable scientific knowledge through reading and by attending seminars and research meetings.Be well organized, detail oriented, able to effectively prioritize, eager to learn, interact cooperatively and effectively with others in a team environment, and consistently demonstrate reliability and responsibility.Able to work independently with minimal supervision as well as collaboratively in team projects.Possess good oral and written communication skills.Possess advanced word processing, data entry, data presentation and analysis computer skills.Comply with standard lab safety practices and standard operating procedures.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).Typical laboratory bending, stooping, lifting requirements apply. Lifting and moving supplies and equipment (up to 25 pounds).  skills: Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $48.68 - 57.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. Independently use appropriate experimental procedure to accomplish an assigned project or design and implement new methodologies to address specific research questions.Prepare technical reports, summaries, protocols, and quantitative analyses of experimental procedures, data, and conclusions. Author and/or edit lab procedures and quality records under Quality Assurance program.Communicates and/or presents results of own work, both oral and written results to supervisor, monthly/annual progress report meetings, and/or project teams. Participates in project planning strategy and overall project execution. May be responsible for a larger project area or multiple smaller projects.Routinely perform and participate in on-going experiments regarding the all assigned programs that also encompass independently designing new or modifying/optimizing current procedures and/or techniques as needed.Develop, design, and implement new procedures by researching and extracting information from scientific literature and/or collaborating or consulting with internal and external personnel to drive progress on research projects.Make detailed observations, record, organize, analyze data, and interpret results in a clear and logical format (e.g., graphs, charts, summaries, etc.). Make routine sound scientific conclusions and decisions within assigned programs; assemble and interpret own data for internal presentations.Recognizes inconsistencies and interprets experimental outcomes. Identify problems with experiments and troubleshoot solutions.Participate in technical transfer of protocols to outsourced companies, provide reagents, and act as troubleshooting contact to external company.Low degree of supervision required within assigned project area.May act as lead worker and be able to train or provide work directions for Research Associate I, II, and/or student interns.Independently implement methods using journal articles and/or other scientists as resources, with a medium degree of supervision.Write and maintain accurate, complete, and timely data in laboratory notebooks.mammalian cells required.Expertise working with virus infectivity assays preferred.Knowledge of theoretical basis and concepts of experimental design and how they fit into overall project goals.Maintain familiarity with current applicable scientific literature and contribute to the process of a project within her/his scientific discipline, as well as investigate, create, and develop new methods and techniques for project advancement.  qualifications: MS Degree in Physical or Life Sciences and 3 years laboratory experience, or BS Degree in Physical or Life Sciences and at least 5 years laboratory experience.Possess a combination of education and experience in a physical and/or life science to work independently, serve as a resource for researchers, train new technicians, and help solve problems with instrument operation.Personal motivation to expand applicable scientific knowledge through reading and by attending seminars and research meetings.Be well organized, detail oriented, able to effectively prioritize, eager to learn, interact cooperatively and effectively with others in a team environment, and consistently demonstrate reliability and responsibility.Able to work independently with minimal supervision as well as collaboratively in team projects.Possess good oral and written communication skills.Possess advanced word processing, data entry, data presentation and analysis computer skills.Comply with standard lab safety practices and standard operating procedures.Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).Typical laboratory bending, stooping, lifting requirements apply. Lifting and moving supplies and equipment (up to 25 pounds).  skills: Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • bedford, massachusetts
    • contract
    • $17 - $20.39 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Bedford, Massachusetts job type: Contract salary: $17.00 - 20.39 per hour work hours: 7 to 3 education: High School   responsibilities: Helps Biocoat package and label product 2-3 days per week and the other 2 days help in Reagents with manual labeling of -20-degree Celsius product.Interacts with Quality Assurance to identify non-conformance issues.Use ETQ to print proper SOPs.Assembles kitsParticipates in other plant activities including Kaizens and 5S blitzes.  qualifications: Highschool diploma or GED. Hard-working attitudeSelf-MotivatedAttention to detailTeam Player Good working conditions.Work in clean rooms, general lab, and cold room ranging from 2 to minus 20 degrees Celsius, where specified PPE for each area is required.Frequently lifts and/or moves material and/or objects up to 50 pounds.Personal Protective Equipment Required: All items will be supplied onsite Lab coatSafety glassesLab gloves   skills: SOP, Quality Assurance Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Bedford, Massachusetts job type: Contract salary: $17.00 - 20.39 per hour work hours: 7 to 3 education: High School   responsibilities: Helps Biocoat package and label product 2-3 days per week and the other 2 days help in Reagents with manual labeling of -20-degree Celsius product.Interacts with Quality Assurance to identify non-conformance issues.Use ETQ to print proper SOPs.Assembles kitsParticipates in other plant activities including Kaizens and 5S blitzes.  qualifications: Highschool diploma or GED. Hard-working attitudeSelf-MotivatedAttention to detailTeam Player Good working conditions.Work in clean rooms, general lab, and cold room ranging from 2 to minus 20 degrees Celsius, where specified PPE for each area is required.Frequently lifts and/or moves material and/or objects up to 50 pounds.Personal Protective Equipment Required: All items will be supplied onsite Lab coatSafety glassesLab gloves   skills: SOP, Quality Assurance Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $16.71 - $19.38 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $16.71 - 19.38 per hour work hours: 9 to 5 education: Associate   responsibilities: Work within Biogen's Gene Therapy Cell Culture Development organization and be engaged in various laboratory aspects. This opportunity grants the individual an opportunity to learn about the bioprocessing application of cell culture and observe how early and late stage drug processes are developed, tested, and transferred to manufacturing scales from lab and pilot scales. The candidate will conduct laboratory cell culture experiments such as setting up and running bench scale bioreactors (sample, analyze, feed, and assess culture performance), shake flasks, micro-scale AMBR bioreactors, as well as large scale bioreactors up to 250L. Experience documenting the laboratory work via the internal electronical lab notebook system will also be acquired. Candidates must be strong team players and have an ability to collaborate effectively on projects. Additionally, the candidate should be strong at troubleshooting and detail oriented. Candidates will be exposed to multiple clinical development programs, new technology projects, and a variety of cell lines, process platforms and cell culture monitoring instrumentation.   qualifications: 2-3 years of engineering or life-science related courses. Self-motivated and team oriented with the ability to work towards independent goals.Excellent organizational and time management skills.Willing to work weekend shifts.Excellent organizational and time management skills.Demonstrated technical proficiency and creativity.Proficient in working with PC based computer systems and relevant applications including Microsoft Excel.Experience with IDBS Electronic Notebook application is a plus.Excellent verbal and written communication skills.Knowledge of and interest in mammalian cell culture techniques including aseptic operations, cell biology, biochemistry, analytical techniques, and bioreactor operations is a plus.  skills: Molecular Biology, MS-EXCEL, Protein Purification, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $16.71 - 19.38 per hour work hours: 9 to 5 education: Associate   responsibilities: Work within Biogen's Gene Therapy Cell Culture Development organization and be engaged in various laboratory aspects. This opportunity grants the individual an opportunity to learn about the bioprocessing application of cell culture and observe how early and late stage drug processes are developed, tested, and transferred to manufacturing scales from lab and pilot scales. The candidate will conduct laboratory cell culture experiments such as setting up and running bench scale bioreactors (sample, analyze, feed, and assess culture performance), shake flasks, micro-scale AMBR bioreactors, as well as large scale bioreactors up to 250L. Experience documenting the laboratory work via the internal electronical lab notebook system will also be acquired. Candidates must be strong team players and have an ability to collaborate effectively on projects. Additionally, the candidate should be strong at troubleshooting and detail oriented. Candidates will be exposed to multiple clinical development programs, new technology projects, and a variety of cell lines, process platforms and cell culture monitoring instrumentation.   qualifications: 2-3 years of engineering or life-science related courses. Self-motivated and team oriented with the ability to work towards independent goals.Excellent organizational and time management skills.Willing to work weekend shifts.Excellent organizational and time management skills.Demonstrated technical proficiency and creativity.Proficient in working with PC based computer systems and relevant applications including Microsoft Excel.Experience with IDBS Electronic Notebook application is a plus.Excellent verbal and written communication skills.Knowledge of and interest in mammalian cell culture techniques including aseptic operations, cell biology, biochemistry, analytical techniques, and bioreactor operations is a plus.  skills: Molecular Biology, MS-EXCEL, Protein Purification, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • temp to perm
    • $20 - $24 per hour
    2nd Shift, Monday- Thursday,  4 PM-2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging  operation is largely a manual operation, with some labeling operations  performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials.  Must follow SOP’s and the ability to follow manufacturing batch records. Understands and complies with cGMP work environment standards and support a strong safety culture. Ability to work in a fast paced work environment while maintaining attention to detail. Ability to work in a team oriented work environment. Willing to work overtime when required.   salary: $20 - $24 per hourshift: Secondwork hours: 4 PM - 2:30 AMeducation: High` SchoolResponsibilities  Responsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging  operation is largely a manual operation, with some labeling operations  performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials.  Must follow SOP’s and the ability to follow manufacturing batch records. Understands and complies with cGMP work environment standards and support a strong safety culture. Ability to work in a fast paced work environment while maintaining attention to detail. Ability to work in a team oriented work environment. Willing to work overtime when required.   SkillsInspectionGMPClean RoomPackagingQuality AssuranceQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    2nd Shift, Monday- Thursday,  4 PM-2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging  operation is largely a manual operation, with some labeling operations  performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials.  Must follow SOP’s and the ability to follow manufacturing batch records. Understands and complies with cGMP work environment standards and support a strong safety culture. Ability to work in a fast paced work environment while maintaining attention to detail. Ability to work in a team oriented work environment. Willing to work overtime when required.   salary: $20 - $24 per hourshift: Secondwork hours: 4 PM - 2:30 AMeducation: High` SchoolResponsibilities  Responsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging  operation is largely a manual operation, with some labeling operations  performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials.  Must follow SOP’s and the ability to follow manufacturing batch records. Understands and complies with cGMP work environment standards and support a strong safety culture. Ability to work in a fast paced work environment while maintaining attention to detail. Ability to work in a team oriented work environment. Willing to work overtime when required.   SkillsInspectionGMPClean RoomPackagingQuality AssuranceQualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $45,000 - $58,000 per year
    2nd shift hours available for Manufacturing Tech II in Billerica, MA The Manufacturing Technician II is responsible for performing manufacturing operations required to produce finished pharmaceutical products, including but not limited to: preparation of chemicals and components, formulation and filling of pharmaceutical products, and operation of various manufacturing equipment (e.g. sterilizers, washers, ovens). salary: $45,000 - $58,000 per yearshift: Secondwork hours: 3 PM - 11:30 PMeducation: High` SchoolResponsibilitiesThis individual will support qualification activities and routine operator maintenance for manufacturing equipment, and will assist with inventory management in designated manufacturing areas.SkillsManufacturing (1 year of experience is required)GMP (1 year of experience is required)aseptic techniques (1 year of experience is preferred)Standard Operating Procedures (1 year of experience is preferred)Batch Records (1 year of experience is preferred)QualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    2nd shift hours available for Manufacturing Tech II in Billerica, MA The Manufacturing Technician II is responsible for performing manufacturing operations required to produce finished pharmaceutical products, including but not limited to: preparation of chemicals and components, formulation and filling of pharmaceutical products, and operation of various manufacturing equipment (e.g. sterilizers, washers, ovens). salary: $45,000 - $58,000 per yearshift: Secondwork hours: 3 PM - 11:30 PMeducation: High` SchoolResponsibilitiesThis individual will support qualification activities and routine operator maintenance for manufacturing equipment, and will assist with inventory management in designated manufacturing areas.SkillsManufacturing (1 year of experience is required)GMP (1 year of experience is required)aseptic techniques (1 year of experience is preferred)Standard Operating Procedures (1 year of experience is preferred)Batch Records (1 year of experience is preferred)QualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lawrence, massachusetts
    • contract
    • $14.45 - $17 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lawrence, Massachusetts job type: Contract salary: $14.45 - 17.00 per hour work hours: 9 to 5 education: High School   responsibilities: Position Description: The Consumable tech will be responsible for manufacturing consumables according to SOP's , meeting company quality and efficiency standards. Position Requirements: - Work in consumable production with group lead or designated trainer - Possess basic manufacturing knowledge - Read, understand and execute SOP's - Basic computer skills - Additional duties as required or directed by the management team   qualifications: Qualifications: - Ability to stand for the duration of shift - Ability to lift 50 pounds - Good written and verbal communication skills - Attention to detail - ISO awareness Education High School Diploma or GED equivalent   skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Lawrence, Massachusetts job type: Contract salary: $14.45 - 17.00 per hour work hours: 9 to 5 education: High School   responsibilities: Position Description: The Consumable tech will be responsible for manufacturing consumables according to SOP's , meeting company quality and efficiency standards. Position Requirements: - Work in consumable production with group lead or designated trainer - Possess basic manufacturing knowledge - Read, understand and execute SOP's - Basic computer skills - Additional duties as required or directed by the management team   qualifications: Qualifications: - Ability to stand for the duration of shift - Ability to lift 50 pounds - Good written and verbal communication skills - Attention to detail - ISO awareness Education High School Diploma or GED equivalent   skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • temp to perm
    • $26 - $32 per hour
    Onsite in Billerica, MA. Great entry level Quality Analyst position for someone with a recent Biology degree or GMP experience.   Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Work in both lab and warehouse areas.  Testing also includes visual inspections, dimensional verifications and analytical testing. 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred. BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience.salary: $26 - $32 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorResponsibilitiesPerform routine QC testing and Visual Inspection in accordance with SOPs and cGMP guidelines. Some supervision required. ·       Perform verification of data to ensure accuracy.  Perform approval upon discretion of supervisor. ·       Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. ·       Utilize a range of electronic systems such as LIMS and document/equipment management software. ·       Author SOP changes; participate in change controls, CAPAs and other quality systems.SkillsQuality AssuranceQuality ControlInspectionQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Onsite in Billerica, MA. Great entry level Quality Analyst position for someone with a recent Biology degree or GMP experience.   Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Work in both lab and warehouse areas.  Testing also includes visual inspections, dimensional verifications and analytical testing. 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred. BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience.salary: $26 - $32 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorResponsibilitiesPerform routine QC testing and Visual Inspection in accordance with SOPs and cGMP guidelines. Some supervision required. ·       Perform verification of data to ensure accuracy.  Perform approval upon discretion of supervisor. ·       Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. ·       Utilize a range of electronic systems such as LIMS and document/equipment management software. ·       Author SOP changes; participate in change controls, CAPAs and other quality systems.SkillsQuality AssuranceQuality ControlInspectionQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $40,000 - $48,000 per year
    Perform GMP cleaning and disinfection services to controlled environments in preparation for manufacturing and research activities.  Perform cleaning and disinfection services within controlled environment manufacturing areas (i.e. clean rooms) to ensure compliance with current Good Manufacturing Practices (cGMP) and US Food and Drug Administration (US FDA).   Maintain the assigned area housekeeping (per cGMP compliance) such as: cleaning walls, floors, doors, drains, windows, and other general surface areas. salary: $40,000 - $48,000 per yearshift: Firstwork hours: 7 AM - 4 PMeducation: High` SchoolResponsibilities 1-3 year(s) experience in cleaning and disinfection services within controlled clean room environments. Ability to understand and execute against cGMP regulations and standard operating procedures (SOPs), and follow verbal and written instructions. Possess knowledge of cleaning and disinfection techniques and use of cleaning and disinfection equipment in a pharmaceutical environment. Demonstrate trouble-shooting and clear communication skills. The incumbent must be able to work in a clean room environment wearing special garments while performing duties. SkillsCleaningQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Perform GMP cleaning and disinfection services to controlled environments in preparation for manufacturing and research activities.  Perform cleaning and disinfection services within controlled environment manufacturing areas (i.e. clean rooms) to ensure compliance with current Good Manufacturing Practices (cGMP) and US Food and Drug Administration (US FDA).   Maintain the assigned area housekeeping (per cGMP compliance) such as: cleaning walls, floors, doors, drains, windows, and other general surface areas. salary: $40,000 - $48,000 per yearshift: Firstwork hours: 7 AM - 4 PMeducation: High` SchoolResponsibilities 1-3 year(s) experience in cleaning and disinfection services within controlled clean room environments. Ability to understand and execute against cGMP regulations and standard operating procedures (SOPs), and follow verbal and written instructions. Possess knowledge of cleaning and disinfection techniques and use of cleaning and disinfection equipment in a pharmaceutical environment. Demonstrate trouble-shooting and clear communication skills. The incumbent must be able to work in a clean room environment wearing special garments while performing duties. SkillsCleaningQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north reading, massachusetts
    • contract
    • $15 - $19.95 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Reading, Massachusetts job type: Contract salary: $15.00 - 19.95 per hour work hours: 9 to 5 education: High School   responsibilities: This position is located in the raw materials warehouse. Primary duties include: Performing visual inspection and labeling of single use components such tubing, filters, and bags used in the manufacturing process.Sampling and labeling of chemicals/biologics in a clean room environment.Performing identification testing using a RAMAN spectrometer.Performing routine maintenance and cleaning of QC areas.Recording data following GMP on paper records, LIMS and SAP.Performing peer review.  qualifications: Requires a high school diploma and a minimum of 0-2 years related experience (Higher degrees may reduce the minimum years' experience required) Knowledge: Little or no knowledge of the job.Moderate understanding of general job aspects and some understanding of the detailed aspects of the job. Key Skills: MS Office, LIMS, SAP, Trackwise, EDMSWorks on assignments that are semi-routine in nature where the ability to recognize deviation from accepted practice is required.Applies job skills and company policies and procedures to complete a variety of tasks. The following physical abilities are required in order to fulfill the job duties: Ability to lift, pull, or push equipment/material requiring 50lbs of forceRepetitive bending and reaching.Ability to work around chemicals  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Reading, Massachusetts job type: Contract salary: $15.00 - 19.95 per hour work hours: 9 to 5 education: High School   responsibilities: This position is located in the raw materials warehouse. Primary duties include: Performing visual inspection and labeling of single use components such tubing, filters, and bags used in the manufacturing process.Sampling and labeling of chemicals/biologics in a clean room environment.Performing identification testing using a RAMAN spectrometer.Performing routine maintenance and cleaning of QC areas.Recording data following GMP on paper records, LIMS and SAP.Performing peer review.  qualifications: Requires a high school diploma and a minimum of 0-2 years related experience (Higher degrees may reduce the minimum years' experience required) Knowledge: Little or no knowledge of the job.Moderate understanding of general job aspects and some understanding of the detailed aspects of the job. Key Skills: MS Office, LIMS, SAP, Trackwise, EDMSWorks on assignments that are semi-routine in nature where the ability to recognize deviation from accepted practice is required.Applies job skills and company policies and procedures to complete a variety of tasks. The following physical abilities are required in order to fulfill the job duties: Ability to lift, pull, or push equipment/material requiring 50lbs of forceRepetitive bending and reaching.Ability to work around chemicals  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, LIMS (Laboratory Information Management System Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $35 - $39.28 per hour
    job summary: The Quality Assurance (QA) Operations department is responsible for quality oversight of operations at company's Framingham Biologics facilities. QA's main responsibility is to ensure adherence to CGMPs during manufacturing operations through partnership with the site and direct engagement with daily operations activities. Quality Assurance Operations is responsible for providing support and guidance to the Company Operations function in order to protect the safety, quality and efficacy of company's products, thereby ensuring the availability of compliant and safe products for our patients and assuring the security of the company's business and global markets. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $35.00 - 39.28 per hour work hours: 7 to 3 education: Bachelors   responsibilities: The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team.Actively supports the QA Operations team by providing technical supportCompletes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change ControlsEnsure all safety requirements are being metPerforms batch record and logbook reviewPerforms review of column packing and qualification recordsReview and approve CRs related to EBRsFunction as SME on challenges related to production requiring quality inputProvide on the floor (OTF) support to the operations department, including OTF support for critical operations stepsIssue action notices and conduct affiliated provisional releaseConduct log book audits against compliance requirementsReview CV related documentation against specificationPerform media / buffer and intermediate releasePerform release of Cell Banks for forward processing (as applicable)Support cross-functional internal audit activities and conduct walkthrough inspectionsExecute containment activitiesProvide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRsMaintain a high level of personal compliance to the required standardsPartner with manufacturing and support operations to ensure a culture of continuous compliance  qualifications: Basic Qualifications: Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field.Knowledge in external agency regulations (FDA, EMA, etc.)Strong computer, verbal and written communication skills.Experience in quality systems.Experience with Trackwise or equivalent system.Proficient in Microsoft Office Preferred Qualifications: Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation.Experience with company Manufacturing System (SMS) or comparable continuous improvement systems.Experience with root cause analysis tools.Demonstrated experience with change control, CAPA and deviation quality systems.Experience in a Quality Assurance role.Strong technical writing skills.Effective time management, attention to detail, organizational skills, teamwork and collaboration.Significant capability in problem solving methodology.Experience training and technically developing employees.Experience participating in external agency inspections.Knowledge of regulatory enforcement trends.Ability to work independently Special Working Conditions: Ability to gown and gain entry to manufacturing and Quality Control areas.Ability to work a 12-hour rotating shift and every other weekend, including holidays.Ability to lift 10 lbs.  skills: MS-WORD, CAPA, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Quality Assurance (QA) Operations department is responsible for quality oversight of operations at company's Framingham Biologics facilities. QA's main responsibility is to ensure adherence to CGMPs during manufacturing operations through partnership with the site and direct engagement with daily operations activities. Quality Assurance Operations is responsible for providing support and guidance to the Company Operations function in order to protect the safety, quality and efficacy of company's products, thereby ensuring the availability of compliant and safe products for our patients and assuring the security of the company's business and global markets. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $35.00 - 39.28 per hour work hours: 7 to 3 education: Bachelors   responsibilities: The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team.Actively supports the QA Operations team by providing technical supportCompletes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change ControlsEnsure all safety requirements are being metPerforms batch record and logbook reviewPerforms review of column packing and qualification recordsReview and approve CRs related to EBRsFunction as SME on challenges related to production requiring quality inputProvide on the floor (OTF) support to the operations department, including OTF support for critical operations stepsIssue action notices and conduct affiliated provisional releaseConduct log book audits against compliance requirementsReview CV related documentation against specificationPerform media / buffer and intermediate releasePerform release of Cell Banks for forward processing (as applicable)Support cross-functional internal audit activities and conduct walkthrough inspectionsExecute containment activitiesProvide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRsMaintain a high level of personal compliance to the required standardsPartner with manufacturing and support operations to ensure a culture of continuous compliance  qualifications: Basic Qualifications: Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field.Knowledge in external agency regulations (FDA, EMA, etc.)Strong computer, verbal and written communication skills.Experience in quality systems.Experience with Trackwise or equivalent system.Proficient in Microsoft Office Preferred Qualifications: Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation.Experience with company Manufacturing System (SMS) or comparable continuous improvement systems.Experience with root cause analysis tools.Demonstrated experience with change control, CAPA and deviation quality systems.Experience in a Quality Assurance role.Strong technical writing skills.Effective time management, attention to detail, organizational skills, teamwork and collaboration.Significant capability in problem solving methodology.Experience training and technically developing employees.Experience participating in external agency inspections.Knowledge of regulatory enforcement trends.Ability to work independently Special Working Conditions: Ability to gown and gain entry to manufacturing and Quality Control areas.Ability to work a 12-hour rotating shift and every other weekend, including holidays.Ability to lift 10 lbs.  skills: MS-WORD, CAPA, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • temp to perm
    • $40 - $65 per hour
    Working with the Head of Total Rewards will collaborate with HR Business Partners to help drive, align and implement the Total Rewards Framework. Key deliverables are to transfer practical compensation knowledge to the HR Business Partners and operationalize total rewards and compensation programs that comply with regulatory requirements, drive business results, employee engagement and enhance our culture. Bachelor’s degree and minimum of 5 years ofdirect compensation experience is required. Understands Long Term Incetive Plans. Understanding of compensation practices and trends. Analytical skills and Excel expertise required. Solid understanding of state and federal wage and hour laws. Ability to exercise judgment and to make decisions independently. Ability to set priorities and manage multiple assignments Exceptional quantitative skills with a commitment to accuracy and details UKG Pro (UltiPro) experience a plussalary: $40 - $65 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities Partner with various stakeholders to support development of career paths and tracks, providing recommendations on compensation matters that both support business goals and ensure market competitiveness regarding application of compensation policies, practices, and guidelines. Maintain and scale job architecture for all employee positions, including job code creating, cleanup and data requests. Integrate new employees seamlessly into the job architecture in the event of a merger or acquisition. Conduct job evaluations and provide salary recommendations ensuring internal equity and market alignment of total compensation while supporting recruitment goals.SkillsCompensationFAS 123r / ASC 718: Compensation - Stock C...Stock PurchaseQualificationsYears of experience: 5 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Working with the Head of Total Rewards will collaborate with HR Business Partners to help drive, align and implement the Total Rewards Framework. Key deliverables are to transfer practical compensation knowledge to the HR Business Partners and operationalize total rewards and compensation programs that comply with regulatory requirements, drive business results, employee engagement and enhance our culture. Bachelor’s degree and minimum of 5 years ofdirect compensation experience is required. Understands Long Term Incetive Plans. Understanding of compensation practices and trends. Analytical skills and Excel expertise required. Solid understanding of state and federal wage and hour laws. Ability to exercise judgment and to make decisions independently. Ability to set priorities and manage multiple assignments Exceptional quantitative skills with a commitment to accuracy and details UKG Pro (UltiPro) experience a plussalary: $40 - $65 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities Partner with various stakeholders to support development of career paths and tracks, providing recommendations on compensation matters that both support business goals and ensure market competitiveness regarding application of compensation policies, practices, and guidelines. Maintain and scale job architecture for all employee positions, including job code creating, cleanup and data requests. Integrate new employees seamlessly into the job architecture in the event of a merger or acquisition. Conduct job evaluations and provide salary recommendations ensuring internal equity and market alignment of total compensation while supporting recruitment goals.SkillsCompensationFAS 123r / ASC 718: Compensation - Stock C...Stock PurchaseQualificationsYears of experience: 5 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts (remote)
    • contract
    • $60 - $85 per hour
    job summary: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $60 - 85 per hour work hours: 9 to 5 education: Doctorate   responsibilities: The Sr. Manager, Medical Information Contact Center Operations - Americas is responsible for supporting and implementing the operations, innovations, and communications strategy for North and Latin America within Global Medical Information (MI). S/He is responsible for overseeing MI frontline services within the United States, Canada, and Latin American regions. Responsibilities will include regional management of Medical Information for the company's COVID-19 vaccine as well as current and future pipeline products in accordance with company policies and procedures and local market regulations. The successful candidate will also be responsible for supporting the development, implementation, and maintenance of the Omni-channel Contact Center (OCCC) for the Americas region including participation in cross-functional planning and operations of Medical Information deliverables and collaboration with key stakeholders. S/He will also provide general OCCC vendor oversight of Medical Information services, including generating, analyzing, and presenting metrics and Key Performance Indicators (KPIs). Maintain strong knowledge of the company's Medical Information policy and processes to ensure compliance across the team.Collaborate with the Medical Information Contact Center (MICC) vendor to support workforce management activities such as:Implementation of the Omni-channel Contact Center structure, including the development, execution, and tracking of metrics and KPIs.Provision of timely, accurate, thorough, and balanced responses to unsolicited requests for information about products from healthcare professionals and consumers consistent with regulatory guidelines utilizing company appropriate information resources.Onboarding new agent access to the Omni-Channel Contact Center programs (AWS and Sales Force Health Cloud).Collaborate with the MI Content, Excursions and Escalations team on training of MICCC personnel and to identify need of new/updated regional content (e.g., Consumer/HCP Frequently Asked Questions (FAQs)).Provide operational metrics with analysis for actionable insights.Remain current on relevant medical/scientific therapeutic areas of interest to the company. Complete all assigned SOPs and training within designated timeframe and adhere to job-specific Standard Operating Procedures (SOPs) and Work Instructions (WI).Attend and staff medical information booth conferences (virtual and in-person) to respond to unsolicited medical information inquiries from HCPs as appropriate.Identify and report potential adverse events (AEs) and product quality complaints (PQCs) to the their respective departments, in accordance with policy and procedures.Support the company Standards, Quality and Compliance group with regulatory inspections and internal audits.  qualifications: Advanced scientific degree (MD, PhD, PharmD) with at least 3 years of biotech and/or pharmaceutical industry preferred; medical information/medical communication experience in the pharmaceutical/biotech industry a plus.Strong understanding of and adherence to regulatory policies governing scientific interactions with HCPs and consumers.Ability to synthesize scientific information for healthcare providers and consumers.Prior industry experience in post-marketing setting; vaccine/infectious disease therapeutic area experience and knowledge strongly preferredCollaborative mindset geared towards working in a team environment where results are achieved through influence and the incorporation of multiple points of viewMotivation to work independently when neededDetail oriented, analytic mind with a strong problem-solving abilityExcellent organizational skills and demonstrated ability to multi-task in a fast-paced environment with changing prioritiesExcellent time management skills and able to manage complexity and to adapt to new circumstances and ideas. Demonstrates an ability to be entrepreneurial and able to work in a highly dynamic environmentAbility to prioritize tasksExcellent written and verbal communication skills  skills: SOP, Vendor Management Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $60 - 85 per hour work hours: 9 to 5 education: Doctorate   responsibilities: The Sr. Manager, Medical Information Contact Center Operations - Americas is responsible for supporting and implementing the operations, innovations, and communications strategy for North and Latin America within Global Medical Information (MI). S/He is responsible for overseeing MI frontline services within the United States, Canada, and Latin American regions. Responsibilities will include regional management of Medical Information for the company's COVID-19 vaccine as well as current and future pipeline products in accordance with company policies and procedures and local market regulations. The successful candidate will also be responsible for supporting the development, implementation, and maintenance of the Omni-channel Contact Center (OCCC) for the Americas region including participation in cross-functional planning and operations of Medical Information deliverables and collaboration with key stakeholders. S/He will also provide general OCCC vendor oversight of Medical Information services, including generating, analyzing, and presenting metrics and Key Performance Indicators (KPIs). Maintain strong knowledge of the company's Medical Information policy and processes to ensure compliance across the team.Collaborate with the Medical Information Contact Center (MICC) vendor to support workforce management activities such as:Implementation of the Omni-channel Contact Center structure, including the development, execution, and tracking of metrics and KPIs.Provision of timely, accurate, thorough, and balanced responses to unsolicited requests for information about products from healthcare professionals and consumers consistent with regulatory guidelines utilizing company appropriate information resources.Onboarding new agent access to the Omni-Channel Contact Center programs (AWS and Sales Force Health Cloud).Collaborate with the MI Content, Excursions and Escalations team on training of MICCC personnel and to identify need of new/updated regional content (e.g., Consumer/HCP Frequently Asked Questions (FAQs)).Provide operational metrics with analysis for actionable insights.Remain current on relevant medical/scientific therapeutic areas of interest to the company. Complete all assigned SOPs and training within designated timeframe and adhere to job-specific Standard Operating Procedures (SOPs) and Work Instructions (WI).Attend and staff medical information booth conferences (virtual and in-person) to respond to unsolicited medical information inquiries from HCPs as appropriate.Identify and report potential adverse events (AEs) and product quality complaints (PQCs) to the their respective departments, in accordance with policy and procedures.Support the company Standards, Quality and Compliance group with regulatory inspections and internal audits.  qualifications: Advanced scientific degree (MD, PhD, PharmD) with at least 3 years of biotech and/or pharmaceutical industry preferred; medical information/medical communication experience in the pharmaceutical/biotech industry a plus.Strong understanding of and adherence to regulatory policies governing scientific interactions with HCPs and consumers.Ability to synthesize scientific information for healthcare providers and consumers.Prior industry experience in post-marketing setting; vaccine/infectious disease therapeutic area experience and knowledge strongly preferredCollaborative mindset geared towards working in a team environment where results are achieved through influence and the incorporation of multiple points of viewMotivation to work independently when neededDetail oriented, analytic mind with a strong problem-solving abilityExcellent organizational skills and demonstrated ability to multi-task in a fast-paced environment with changing prioritiesExcellent time management skills and able to manage complexity and to adapt to new circumstances and ideas. Demonstrates an ability to be entrepreneurial and able to work in a highly dynamic environmentAbility to prioritize tasksExcellent written and verbal communication skills  skills: SOP, Vendor Management Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • cambridge, massachusetts
    • contract
    • $28.64 - $33.69 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $28.64 - 33.69 per hour work hours: 9 to 5 education: High School   responsibilities: Provides comprehensive administrative support for Heads of Trial Insights and Performance, and Clinical Partner Management, as well as their leadership team.Coordinate key meetings like Town Halls and interactions with leaders from other Takeda functions.Coordinate and schedule key training events and also work with functional leads for the generation of our quarterly newsletterSupports special projects and activities for GDO functionsUses appropriate tools for required work including Microsoft Outlook, Word, Excel, and Power Point to track, analyze, document, and report data.Reviews documents and proofreads work for grammar and spelling, accuracy, consistency of terms, and completeness; ensures document text and graphics adhere to corporate and organization guidelines and standards.Arranges travel; completes expense reports in a timely manner.Collects, reviews, analyzes, interprets, enters, and formats accurate data into intranet, spreadsheets, databases and other electronic tools.Interfaces and communicates with internal and external customers; directs people to the appropriate resources.Researches solutions and responds to email and phone inquiries with minimal input from direct supervisor; interacts effectively with all levels of employees throughout the company.Supports the administrative needs of Trial Insights and Performance, as well as Clinical Partner Management groupsManage event planning of key leadership meetings (e.g. GDO Town Hall) with autonomy including logistics, execution and post-meeting follow-upSupport creation of key communication to GDO organization and lead dissemination of communication including managing GDO mailbox & distribution listsCoordinate logistics and support team workshops and meetings including liaising with IT support for technology needsSchedules meetings, calls, and other interactions based on the priorities of the leader and/or function.Initiates, develops, leads, and participates in improvement processes; actively participates in resulting process improvements.Understands the structure of the organization and develops a strong network across departments; draws on network to answer questions, solve problems, and successfully execute responsibilities.Demonstrates confidentiality in execution of all responsibilities.Performs other duties as required.  qualifications: High school diploma/GED required. Associates degree or bachelor's degree preferred.Minimum 8 years of relevant work experience, or equivalent combination of training and experience. Some industry experience is preferred.Strong PC literacy with advanced skills in Microsoft Outlook, Word, Excel, or PowerPoint.Excellent verbal and written communication skills.Ability to identify more complex issues that require escalation for resolutionFully understand importance of data integrity and attention to detailDemonstrated ability to independently pursue and follow-up on assignments and issues through completionDetail orientation with the demonstrated ability to multi-taskDemonstrates well developed administrative / project organizational skills Demonstrates ability to plan and execute team events and meetings  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Administration, Calendar Management, Expense Reporting, File Management Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Cambridge, Massachusetts job type: Contract salary: $28.64 - 33.69 per hour work hours: 9 to 5 education: High School   responsibilities: Provides comprehensive administrative support for Heads of Trial Insights and Performance, and Clinical Partner Management, as well as their leadership team.Coordinate key meetings like Town Halls and interactions with leaders from other Takeda functions.Coordinate and schedule key training events and also work with functional leads for the generation of our quarterly newsletterSupports special projects and activities for GDO functionsUses appropriate tools for required work including Microsoft Outlook, Word, Excel, and Power Point to track, analyze, document, and report data.Reviews documents and proofreads work for grammar and spelling, accuracy, consistency of terms, and completeness; ensures document text and graphics adhere to corporate and organization guidelines and standards.Arranges travel; completes expense reports in a timely manner.Collects, reviews, analyzes, interprets, enters, and formats accurate data into intranet, spreadsheets, databases and other electronic tools.Interfaces and communicates with internal and external customers; directs people to the appropriate resources.Researches solutions and responds to email and phone inquiries with minimal input from direct supervisor; interacts effectively with all levels of employees throughout the company.Supports the administrative needs of Trial Insights and Performance, as well as Clinical Partner Management groupsManage event planning of key leadership meetings (e.g. GDO Town Hall) with autonomy including logistics, execution and post-meeting follow-upSupport creation of key communication to GDO organization and lead dissemination of communication including managing GDO mailbox & distribution listsCoordinate logistics and support team workshops and meetings including liaising with IT support for technology needsSchedules meetings, calls, and other interactions based on the priorities of the leader and/or function.Initiates, develops, leads, and participates in improvement processes; actively participates in resulting process improvements.Understands the structure of the organization and develops a strong network across departments; draws on network to answer questions, solve problems, and successfully execute responsibilities.Demonstrates confidentiality in execution of all responsibilities.Performs other duties as required.  qualifications: High school diploma/GED required. Associates degree or bachelor's degree preferred.Minimum 8 years of relevant work experience, or equivalent combination of training and experience. Some industry experience is preferred.Strong PC literacy with advanced skills in Microsoft Outlook, Word, Excel, or PowerPoint.Excellent verbal and written communication skills.Ability to identify more complex issues that require escalation for resolutionFully understand importance of data integrity and attention to detailDemonstrated ability to independently pursue and follow-up on assignments and issues through completionDetail orientation with the demonstrated ability to multi-taskDemonstrates well developed administrative / project organizational skills Demonstrates ability to plan and execute team events and meetings  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Administration, Calendar Management, Expense Reporting, File Management Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • north billerica, massachusetts
    • permanent
    • $52 - $70 per year
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Billerica, Massachusetts job type: Permanent salary: $52 - 70 per year work hours: 9 to 5 education: Associate   responsibilities: The Quality Document Specialist is an individual contributor who is responsible for conducting day to day processing of document workflows for cGMP operations. Will assist with ongoing quality documentation deliverables driven by business objectives and identified by management. Coordinates, authors, proofreads, formats, troubleshoots issues and distributes controlled documents supporting the manufacturing and testing of products.Balance and prioritize assigned workload to meet requested timelines.Aligns with all levels of the organization to meet the needs of documentation system users on site and at external facilities.Manages multiple tasks in a fast paced and dynamic environment while maintaining focus on quality and compliance with local SOPs, policies and directives, and regulatory requirements.Supports individual and group training sessions for system users on making document changes and reviewing electronic references copies of documents.Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards.Actively demonstrates the company values of accountability, quality, efficiency, customer service, collaboration and safety. * In the case of absence the reports to Manager above or a peer incumbent will function as a backup for this position.   qualifications: AS in English or Science.A combination of education, training and experience may be considered in lieu of the above stated qualifications.4-6 years of experience in the pharmaceutical industry, preferably within quality or Documentation function Prior experience with Electronic Documentation Management System is preferredProficient in Microsoft ExcelProficient in advanced functions of Microsoft Word Excellent verbal and written communication Ability to work independently to resolve issues and meet the required issue date for documents Ability to work in a team environment Attention to detailSome overtime may be required.  skills: Quality control, SOP, MS-WORD, MS-EXCEL, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: North Billerica, Massachusetts job type: Permanent salary: $52 - 70 per year work hours: 9 to 5 education: Associate   responsibilities: The Quality Document Specialist is an individual contributor who is responsible for conducting day to day processing of document workflows for cGMP operations. Will assist with ongoing quality documentation deliverables driven by business objectives and identified by management. Coordinates, authors, proofreads, formats, troubleshoots issues and distributes controlled documents supporting the manufacturing and testing of products.Balance and prioritize assigned workload to meet requested timelines.Aligns with all levels of the organization to meet the needs of documentation system users on site and at external facilities.Manages multiple tasks in a fast paced and dynamic environment while maintaining focus on quality and compliance with local SOPs, policies and directives, and regulatory requirements.Supports individual and group training sessions for system users on making document changes and reviewing electronic references copies of documents.Actively promotes safety rules and awareness. Demonstrates good safety practices at all times including the appropriate use of protective equipment. Reports and takes initiative to correct safety & environmental hazards.Actively demonstrates the company values of accountability, quality, efficiency, customer service, collaboration and safety. * In the case of absence the reports to Manager above or a peer incumbent will function as a backup for this position.   qualifications: AS in English or Science.A combination of education, training and experience may be considered in lieu of the above stated qualifications.4-6 years of experience in the pharmaceutical industry, preferably within quality or Documentation function Prior experience with Electronic Documentation Management System is preferredProficient in Microsoft ExcelProficient in advanced functions of Microsoft Word Excellent verbal and written communication Ability to work independently to resolve issues and meet the required issue date for documents Ability to work in a team environment Attention to detailSome overtime may be required.  skills: Quality control, SOP, MS-WORD, MS-EXCEL, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • lexington, massachusetts
    • temp to perm
    • $28 - $29 per hour
    Takeda Pharmaceuticals is currently hiring for a number of Manufacturing Associate openings in their Contingent Core Team program.  These would be contract to hire positions supporting multiple groups, providing exposure to both downstream and upstream operations.   Flexibility to commute to both Cambridge and Lexington is required. Multiple day shift (6am-6:30pm) and night shift (6pm-6:30am) openings available.salary: $28 - $29 per hourshift: Firstwork hours: 6 AM - 6:30 PMeducation: High` SchoolResponsibilitiesThe individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Records and Form Preps. Primary responsibilities include: • Execution of activities in support of production • Perform requests and execution of GMP documentation • Enter data in the Laboratory Information Management System (LIMS), MODA and or other business systems • Sample preparation and testing • Complete required training on time • Carry out work in a safe manner, notifying management of safety issues and risks • Participate in tiered visual management system The individual will manage equipment and support facility related projects by: • recognize issues and escalate to senior staff • Perform scheduled cleaning of equipment • Perform standardization of equipment • Support change over activities • Assist in the assembly and disassembly of process equipment • Staff Technical Training and Development • Maintain training requirements • Develop and maintain personal development planThe essential functions of this role include:working in a smoke free environmentstanding for 8 hours at one timeworking up to 8 hrs of overtime per weekworking weekendsSkillscGMPSOPsattention to detailCommunicationQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    Takeda Pharmaceuticals is currently hiring for a number of Manufacturing Associate openings in their Contingent Core Team program.  These would be contract to hire positions supporting multiple groups, providing exposure to both downstream and upstream operations.   Flexibility to commute to both Cambridge and Lexington is required. Multiple day shift (6am-6:30pm) and night shift (6pm-6:30am) openings available.salary: $28 - $29 per hourshift: Firstwork hours: 6 AM - 6:30 PMeducation: High` SchoolResponsibilitiesThe individual will carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOP), Batch Records and Form Preps. Primary responsibilities include: • Execution of activities in support of production • Perform requests and execution of GMP documentation • Enter data in the Laboratory Information Management System (LIMS), MODA and or other business systems • Sample preparation and testing • Complete required training on time • Carry out work in a safe manner, notifying management of safety issues and risks • Participate in tiered visual management system The individual will manage equipment and support facility related projects by: • recognize issues and escalate to senior staff • Perform scheduled cleaning of equipment • Perform standardization of equipment • Support change over activities • Assist in the assembly and disassembly of process equipment • Staff Technical Training and Development • Maintain training requirements • Develop and maintain personal development planThe essential functions of this role include:working in a smoke free environmentstanding for 8 hours at one timeworking up to 8 hrs of overtime per weekworking weekendsSkillscGMPSOPsattention to detailCommunicationQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
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