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    • waukegan, illinois (remote)
    • contract
    • $35 - $37.62 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Waukegan, Illinois job type: Contract salary: $35.00 - 37.62 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Initiate, investigate, and maintain complaint files following complaint handling regulation 21 CFR 820.198 and internal procedures. Analyze information obtained and make follow calls to reporters. Initiate and set up complaint files. Maintain and update database. Record all complaint activity in both hard copy (when applicable) and computer files. Code complaint information according to Post Market Spreadsheet Report (PSR), Retrieval Program.Assess incoming documentation, including clinical forms and medical information, for complaint data and ascertain compliance to product specification and/or intended use as indicated in the product labeling. Evaluate internal and external lab analysis. Coordinate with inter- and intra-departmental customers to ensure complaints and inquiries across product lines are handled appropriately.Initiate Further Investigation and any additional follow-up and communication pertinent to the MDR as needed. Track files sent to Quality Assurance for Further Investigation and complete necessary documentation. Evaluate Further Investigation results, summarize findings, and determine and document the conclusion(s).Assist Supervisors and Manager in monitoring complaint and claims workflow to ensure compliance and customer service.Assist in resolving issues by responding to inquiries and answering technical questions regarding Company's product line.  qualifications: Bachelor's degree with one to two years previous experience in customer service or clinical setting or equivalent combination of education and experience.Customer service experienceFamiliarity with Regulation pertaining to devices/510K (i.e. FDA, MHRA, etc.)Flexibility in managing multiple tasks and expectations  skills: MS-WORD, MS-EXCEL 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Waukegan, Illinois job type: Contract salary: $35.00 - 37.62 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Initiate, investigate, and maintain complaint files following complaint handling regulation 21 CFR 820.198 and internal procedures. Analyze information obtained and make follow calls to reporters. Initiate and set up complaint files. Maintain and update database. Record all complaint activity in both hard copy (when applicable) and computer files. Code complaint information according to Post Market Spreadsheet Report (PSR), Retrieval Program.Assess incoming documentation, including clinical forms and medical information, for complaint data and ascertain compliance to product specification and/or intended use as indicated in the product labeling. Evaluate internal and external lab analysis. Coordinate with inter- and intra-departmental customers to ensure complaints and inquiries across product lines are handled appropriately.Initiate Further Investigation and any additional follow-up and communication pertinent to the MDR as needed. Track files sent to Quality Assurance for Further Investigation and complete necessary documentation. Evaluate Further Investigation results, summarize findings, and determine and document the conclusion(s).Assist Supervisors and Manager in monitoring complaint and claims workflow to ensure compliance and customer service.Assist in resolving issues by responding to inquiries and answering technical questions regarding Company's product line.  qualifications: Bachelor's degree with one to two years previous experience in customer service or clinical setting or equivalent combination of education and experience.Customer service experienceFamiliarity with Regulation pertaining to devices/510K (i.e. FDA, MHRA, etc.)Flexibility in managing multiple tasks and expectations  skills: MS-WORD, MS-EXCEL 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 chicago, illinois (remote)
    • contract
    • $55 - $62.51 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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 Chicago, Illinois job type: Contract salary: $55.00 - 62.51 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Develops and maintains US/EU package inserts and Company Core Data Sheets and coordinates review and approval of these documents with changing regulatory environments. Leads discussions to ensure global consistency of labeling. Educates team members concerning global consistency of labeling.Leads teams on labeling decisions based on knowledge of processes and regulations. Educates others as to new labeling regulations regarding Company core Data Sheet (CCDS), US Package Insert (USPI), Summary of Product Characteristics (SmPC), Structured Product Labeling (SPL), or Instructions for Use (IFUs)Reviews and assesses data to determine whether accurate and reproducible. Works with clinical and safety teams to assure revised data is included as support documentation following approvals. Provides labeling input for Risk Management Plans, Regulatory Strategic & Tactical Plans (RSTPs) and safety documentsDrives strategic labeling processes within teams based on knowledge of success with other products. Makes recommendations to proactively optimize label language, including effective use of Target Product Label (TPL) and Development Core Data Sheets (DCDS) as applicable, for assigned productsMaintains accurate files of labeling change history and associated documents, including annotations to data sourcesParticipates at team meetings, reviews materials, authors documents and meets timelines. Leads cross-functional teams to resolve labeling issues and address Ministry of Health (MOH) requests globallyWorks with safety groups on safety issues and leads discussion on safety related labeling changes. Makes decisions on own topics and those of direct reports based on experience with various products. Understands and supports regulatory implications of product profile.Works strategically with R&D, Global Medical Affairs and safety to maintain accurate safety profiles for assigned productsWorks with Labeling Operations to ensure quality documents are internally maintained or submitted to FDA Provides labeling support to Asset Development Team (ADTs) and affiliates including pre-approvals, renewals, and competitive analysisMay indirectly manage work of other department members. Assists in training of new personnel and in the development of department processes/policies.  qualifications: Required Education: Bachelor's degree in Pharmacy, Biology, Chemistry, pharmacology or related subjectPreferred Education: Bachelor's degree. Certifications a plusRequired Experience: 6 years in Pharmaceutical, regulatory, R&D or industry related area. Experience in labeling or area that could link to labelingAbility to supervise projects and set daily priorities. Able to work in a complex and matrix environmentPreferred Experience: 3 years in pharmaceutical or regulatory preferred. Minimum 3 years' experience in clinical or pharmaceutical preferredCross-divisional team experience and working with cross-functional teamsStrong problem solving with minimal guidance  skills: FDA, MS-WORD, MS-EXCEL, MS-Powerpoint, 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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 Chicago, Illinois job type: Contract salary: $55.00 - 62.51 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Develops and maintains US/EU package inserts and Company Core Data Sheets and coordinates review and approval of these documents with changing regulatory environments. Leads discussions to ensure global consistency of labeling. Educates team members concerning global consistency of labeling.Leads teams on labeling decisions based on knowledge of processes and regulations. Educates others as to new labeling regulations regarding Company core Data Sheet (CCDS), US Package Insert (USPI), Summary of Product Characteristics (SmPC), Structured Product Labeling (SPL), or Instructions for Use (IFUs)Reviews and assesses data to determine whether accurate and reproducible. Works with clinical and safety teams to assure revised data is included as support documentation following approvals. Provides labeling input for Risk Management Plans, Regulatory Strategic & Tactical Plans (RSTPs) and safety documentsDrives strategic labeling processes within teams based on knowledge of success with other products. Makes recommendations to proactively optimize label language, including effective use of Target Product Label (TPL) and Development Core Data Sheets (DCDS) as applicable, for assigned productsMaintains accurate files of labeling change history and associated documents, including annotations to data sourcesParticipates at team meetings, reviews materials, authors documents and meets timelines. Leads cross-functional teams to resolve labeling issues and address Ministry of Health (MOH) requests globallyWorks with safety groups on safety issues and leads discussion on safety related labeling changes. Makes decisions on own topics and those of direct reports based on experience with various products. Understands and supports regulatory implications of product profile.Works strategically with R&D, Global Medical Affairs and safety to maintain accurate safety profiles for assigned productsWorks with Labeling Operations to ensure quality documents are internally maintained or submitted to FDA Provides labeling support to Asset Development Team (ADTs) and affiliates including pre-approvals, renewals, and competitive analysisMay indirectly manage work of other department members. Assists in training of new personnel and in the development of department processes/policies.  qualifications: Required Education: Bachelor's degree in Pharmacy, Biology, Chemistry, pharmacology or related subjectPreferred Education: Bachelor's degree. Certifications a plusRequired Experience: 6 years in Pharmaceutical, regulatory, R&D or industry related area. Experience in labeling or area that could link to labelingAbility to supervise projects and set daily priorities. Able to work in a complex and matrix environmentPreferred Experience: 3 years in pharmaceutical or regulatory preferred. Minimum 3 years' experience in clinical or pharmaceutical preferredCross-divisional team experience and working with cross-functional teamsStrong problem solving with minimal guidance  skills: FDA, MS-WORD, MS-EXCEL, MS-Powerpoint, 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.
    • ankeny, iowa
    • temporary
    • $17 - $19 per hour
    Randstad is seeking a Lab Technician to work with our client in Ankeny, Iowa. As the selected candidate, you will be working in their Seed Chipping Lab.  For this position you will need 1-3 years of experience working in a lab environment. An Associates or Bachelor's degree in a scientific discipline is preferred.  salary: $17 - $19 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities Performs laboratory technical tasks.Responsible for the care and maintenance of automated laboratory equipment.Will be required to offer assistance in the operation of the equipment and the gathering of data.Assists with receipt and inspection of raw materials, ordering and stocking.Has knowledge of commonly-used concepts, practices, and procedures within a particular field.Relies on instructions and pre-established guidelines to perform the functions of the job. Skills Laboratory Testing (1 year of experience is required)Lab Automations (1 year of experience is required) Qualifications Years of experience: 1 yearExperience level: Experienced Randstad 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.
    Randstad is seeking a Lab Technician to work with our client in Ankeny, Iowa. As the selected candidate, you will be working in their Seed Chipping Lab.  For this position you will need 1-3 years of experience working in a lab environment. An Associates or Bachelor's degree in a scientific discipline is preferred.  salary: $17 - $19 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities Performs laboratory technical tasks.Responsible for the care and maintenance of automated laboratory equipment.Will be required to offer assistance in the operation of the equipment and the gathering of data.Assists with receipt and inspection of raw materials, ordering and stocking.Has knowledge of commonly-used concepts, practices, and procedures within a particular field.Relies on instructions and pre-established guidelines to perform the functions of the job. Skills Laboratory Testing (1 year of experience is required)Lab Automations (1 year of experience is required) Qualifications Years of experience: 1 yearExperience level: Experienced Randstad 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
    • $32 - $38.55 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: $32.00 - 38.55 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Write and maintain accurate, complete, and timely data in laboratory notebooks. - Independently design specific laboratory experiments. - Prepare technical reports, summaries, protocols, and quantitative analyses of experimental procedures, data, and conclusions. - Effectively communicate results of experiments and analyses to supervisor and/or project teams. Perform routine scientific experiments independently and be responsible for research and development in collaboration with others on projects. - Perform new procedures with only general instructions. - Make detailed observations, organize and analyze data, and interpret results in a clear and logical format (e.g., graphs, charts, summaries). - Identify problems with experiments and troubleshoot solutions with guidance from supervisor. Good understanding of basic experimental objectives and concepts of experimental design. - 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. - Personal motivation to expand applicable scientific knowledge through reading and by attending seminars and research meetings. - Possess working knowledge of mammalian cell culture and sterile transfer technique - Possess familiarity with cell enumeration and fluorescent staining - Possess ability to set up and operate bench-top cell culture bioreactors - May be required to occasionally work during evening or weekend hours   qualifications: - Be well organized and detail oriented, effectively prioritize, eager to learn, interact cooperatively and effectively with others in a team environment, and consistently demonstrate reliability and responsibility. - Possess good oral and written communication skills. - Possess advanced word processing, data entry, data presentation and analysis computer skills. - Comply with company safety practices and standard operating procedures. - Exhibit and promote company Core Competencies. - BS Degree in Physical or Life Sciences and 1-3 years laboratory experience, or MS Degree in Physical or Life Sciences and 0-2 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. - 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: MS-WORD, MS-EXCEL, 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 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: $32.00 - 38.55 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Write and maintain accurate, complete, and timely data in laboratory notebooks. - Independently design specific laboratory experiments. - Prepare technical reports, summaries, protocols, and quantitative analyses of experimental procedures, data, and conclusions. - Effectively communicate results of experiments and analyses to supervisor and/or project teams. Perform routine scientific experiments independently and be responsible for research and development in collaboration with others on projects. - Perform new procedures with only general instructions. - Make detailed observations, organize and analyze data, and interpret results in a clear and logical format (e.g., graphs, charts, summaries). - Identify problems with experiments and troubleshoot solutions with guidance from supervisor. Good understanding of basic experimental objectives and concepts of experimental design. - 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. - Personal motivation to expand applicable scientific knowledge through reading and by attending seminars and research meetings. - Possess working knowledge of mammalian cell culture and sterile transfer technique - Possess familiarity with cell enumeration and fluorescent staining - Possess ability to set up and operate bench-top cell culture bioreactors - May be required to occasionally work during evening or weekend hours   qualifications: - Be well organized and detail oriented, effectively prioritize, eager to learn, interact cooperatively and effectively with others in a team environment, and consistently demonstrate reliability and responsibility. - Possess good oral and written communication skills. - Possess advanced word processing, data entry, data presentation and analysis computer skills. - Comply with company safety practices and standard operating procedures. - Exhibit and promote company Core Competencies. - BS Degree in Physical or Life Sciences and 1-3 years laboratory experience, or MS Degree in Physical or Life Sciences and 0-2 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. - 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: MS-WORD, MS-EXCEL, 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.
    • chesterfield, missouri
    • temporary
    • $25 - $30 per hour
    Randstad is seeking a talented and experienced Biologist with a background in Plant Molecular Biology.  This position is with our client, a global leader in agricultural research. They are shaping the world of agriculture with breakthrough innovation for the benefit of farmers, consumers and our planet.What you need: You should have a degree in Plant Biology, Molecular Biology, Cell Biology, Biochemistry or other related field with 3+ years of laboratory experience. Candidates with Master or PhD degrees are desired. Tissue culture, aseptic technique, plant transformation, and genome editing experience.Computer proficiency, particularly with Microsoft Office, Excel, database, data analysis software and basic bioinformatics tools. salary: $25 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesAs the selecte candidate, you will be expected to routinely handle the growth and maintenance of crops; assist in the design and execution and documentation of experiments in the laboratory and controlled environment. You will need the ability to interpret experimental results.. This position requires a highly motivated and results-oriented team player with excellent oral and written communication skills and scientific depth.  Skills Tissue Culture (3 years of experience is required)Plant Transformation (3 years of experience is required)Greenhouse/Growth Chamber (3 years of experience is required)Genome Editing (3 years of experience is required)Data Analysis (3 years of experience is required)Experimental Design (3 years of experience is required) Qualifications Years of experience: 3 yearsExperience level: Experienced Randstad 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.
    Randstad is seeking a talented and experienced Biologist with a background in Plant Molecular Biology.  This position is with our client, a global leader in agricultural research. They are shaping the world of agriculture with breakthrough innovation for the benefit of farmers, consumers and our planet.What you need: You should have a degree in Plant Biology, Molecular Biology, Cell Biology, Biochemistry or other related field with 3+ years of laboratory experience. Candidates with Master or PhD degrees are desired. Tissue culture, aseptic technique, plant transformation, and genome editing experience.Computer proficiency, particularly with Microsoft Office, Excel, database, data analysis software and basic bioinformatics tools. salary: $25 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesAs the selecte candidate, you will be expected to routinely handle the growth and maintenance of crops; assist in the design and execution and documentation of experiments in the laboratory and controlled environment. You will need the ability to interpret experimental results.. This position requires a highly motivated and results-oriented team player with excellent oral and written communication skills and scientific depth.  Skills Tissue Culture (3 years of experience is required)Plant Transformation (3 years of experience is required)Greenhouse/Growth Chamber (3 years of experience is required)Genome Editing (3 years of experience is required)Data Analysis (3 years of experience is required)Experimental Design (3 years of experience is required) Qualifications Years of experience: 3 yearsExperience level: Experienced Randstad 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 chicago, illinois
    • contract
    • $65 - $77.72 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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 Chicago, Illinois job type: Contract salary: $65.00 - 77.72 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and Company policies and procedures).Leader of the cross functional study team: o Leads Clinical Study Execution Team Meetings o Project manager for clinical studies leveraging the clinical schedule; manages the critical path and milestonesResponsible for the vendor/CRO selection, scope development, management and oversight of external vendors/CROs in compliance with Company's processes and procedures and the applicable regulationsResponsible for regular updates to the cross-functional team and stakeholders on study status; ensures our CTMS is up to dateResponsible for the development of the clinical study design and associated systems and documents (for example: Informed consent forms, eCRFs, IRT, CSR)Responsible for study budget creation and oversight of spend against approved budgetResponsible for generating the study related training for the study team, study sites, and vendors for assigned studiesProactively identify and address and/or escalate study related issues and opportunities for efficiencyDecision maker on operational aspects of study execution. Participates in innovation and process improvement initiatives. Provides direct supervision of study management associate(s) including career development of clinical operations staff and creating an inclusive and innovative environment where staff and studies/programs will succeed.  qualifications: Bachelor's Degree or OUS equivalent degree is required, typically in nursing or scientific field; Registered Nurse licensure with Associates Degree in Nursing with relevant experience is also acceptable.Must have at least 6 years of Pharma-related/clinical research related experience.Strong background leading oncology clinical trialsExperience overseeing fully outsourced clinical trials or experience at a CRODemonstrates a high level of core and technical competencies through management of various components of clinical trials.Possesses good communication skills and demonstrated leadership abilities.Demonstration of successful coaching/mentoring in a matrix environment.Competent in application of standard business procedures (Standard Operating Procedures, International Conference on Harmonization (ICH), Global Regulations, Ethics and Compliance).Preferred exposure in study initiation through study completion in multiple phases of studies.  skills: MS-WORD, MS-EXCEL, CRFs, GCP (Good Clinical Practice), Portfolio Management, Study Planning, CTMS (Clinical Trial Management Systems), 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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 Chicago, Illinois job type: Contract salary: $65.00 - 77.72 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and Company policies and procedures).Leader of the cross functional study team: o Leads Clinical Study Execution Team Meetings o Project manager for clinical studies leveraging the clinical schedule; manages the critical path and milestonesResponsible for the vendor/CRO selection, scope development, management and oversight of external vendors/CROs in compliance with Company's processes and procedures and the applicable regulationsResponsible for regular updates to the cross-functional team and stakeholders on study status; ensures our CTMS is up to dateResponsible for the development of the clinical study design and associated systems and documents (for example: Informed consent forms, eCRFs, IRT, CSR)Responsible for study budget creation and oversight of spend against approved budgetResponsible for generating the study related training for the study team, study sites, and vendors for assigned studiesProactively identify and address and/or escalate study related issues and opportunities for efficiencyDecision maker on operational aspects of study execution. Participates in innovation and process improvement initiatives. Provides direct supervision of study management associate(s) including career development of clinical operations staff and creating an inclusive and innovative environment where staff and studies/programs will succeed.  qualifications: Bachelor's Degree or OUS equivalent degree is required, typically in nursing or scientific field; Registered Nurse licensure with Associates Degree in Nursing with relevant experience is also acceptable.Must have at least 6 years of Pharma-related/clinical research related experience.Strong background leading oncology clinical trialsExperience overseeing fully outsourced clinical trials or experience at a CRODemonstrates a high level of core and technical competencies through management of various components of clinical trials.Possesses good communication skills and demonstrated leadership abilities.Demonstration of successful coaching/mentoring in a matrix environment.Competent in application of standard business procedures (Standard Operating Procedures, International Conference on Harmonization (ICH), Global Regulations, Ethics and Compliance).Preferred exposure in study initiation through study completion in multiple phases of studies.  skills: MS-WORD, MS-EXCEL, CRFs, GCP (Good Clinical Practice), Portfolio Management, Study Planning, CTMS (Clinical Trial Management Systems), 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.
    • north wales, pennsylvania (remote)
    • contract
    • $130 - $150 per hour
    job summary: Exciting opportunity to join a world-class CRO as a senior/principal biostatistician, fully remote!   location: North Wales, Pennsylvania job type: Contract salary: $130 - 150 per hour work hours: 9 to 5 education: Masters   responsibilities: Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies.Serves as an independent reporting statistician on data monitoring committees.Develops statistical analysis plans and reporting specifications for simple to complex clinical studies.Reviews statistical analyses of other statisticians and interprets results from simple to complex clinical studies.Performs senior review of TFLs and statistical analysis plans.Provides significant input in the development and review of CRFs, edit specifications, and critical variable lists.  qualifications: Master's degree in statistics or biostatistics required. PhD preferred. Minimum of 6 years of biostatistical experience desired.Oncology experience preferredExhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices.Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials.  skills: Biostatistical Analysis 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: Exciting opportunity to join a world-class CRO as a senior/principal biostatistician, fully remote!   location: North Wales, Pennsylvania job type: Contract salary: $130 - 150 per hour work hours: 9 to 5 education: Masters   responsibilities: Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies.Serves as an independent reporting statistician on data monitoring committees.Develops statistical analysis plans and reporting specifications for simple to complex clinical studies.Reviews statistical analyses of other statisticians and interprets results from simple to complex clinical studies.Performs senior review of TFLs and statistical analysis plans.Provides significant input in the development and review of CRFs, edit specifications, and critical variable lists.  qualifications: Master's degree in statistics or biostatistics required. PhD preferred. Minimum of 6 years of biostatistical experience desired.Oncology experience preferredExhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices.Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials.  skills: Biostatistical Analysis 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.
    • watertown, massachusetts
    • permanent
    • $190,000 - $210,000 per year
    job summary: Watertown MA based company who provides novel solutions to clients for advanced therapy process development and manufacturing which is establishing the first end-to-end manufacturing capability for mRNA is actively seeking (1) Director of Drug Product Fill/Finish Manufacturing starting ASAP!! This is a full-time Permanent opportunity with flexible day shift hours, no weekends. The Director of Product Manufacturing will lead the establishment of the full Fill/Finish value chain for the company. This person is responsible for building, maintaining, and continuously improving a highly effective Fill/Finish capability including filling, visual inspection, labelling, and packaging operations for mRNA as well as a variety of sterile parenteral products using state-of-the-art equipment. They will provide the leadership, management, and vision necessary to ensure that the company has the proper controls, KPI, people, and systems in place within the Fill/Finish and manufacturing function. Great location which has numerous attractions including dozens of excellent shopping spots, restaurants, museums, historical sites, colleges and much more. Located of the Mass Pike and their are plenty of commuter rail stops for commuters!!   location: Watertown, Massachusetts job type: Permanent salary: $190,000 - 210,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Direct all day-to-day fill-finish manufacturing operating including but not limited to aseptic filling and product labeling and packaging to ensure delivery of departmental commitments to achieve company objectivesEstablish a Best-in-Class Fill/Finish value chain for the company and its clientsDevelop a robust visual inspection training program/strategyDirect all planning, scheduling, and production functions to ensure adequate materials, equipment, and personnel are available to meet the production scheduleEncourage and enforce a culture of compliance and continuous improvement regarding Safety and QualityDevelops and implements Key Performance Indicators to track and lead successful, timely achievement of goals, objectives, and projectsMaintains departmental operational and capital budget, responsible for driving financial results, drives optimization of fixed and variable costProvide leadership and direction to ensure Inspections, Deviations, Change Control, CAPAs and Regulatory commitments are met on time with the highest standards of qualityEvaluate the functional strengths and developmental areas in the GMP manufacturing team and focuses on continuous improvement.Must stay current with relevant technologies and forward thinking to identify new approachesDirect all day-to-day Fill and Finish manufacturing operations including but not limited to manufacturing, manufacturing support, & manufacturing compliance to ensure delivery of departmental commitments to achieve company objectivesDirect all planning, scheduling, and production functions to ensure adequate materials, equipment, and personnel are available to meet the production scheduleEvaluate the functional strengths and developmental areas in the GMP manufacturing team and focuses on continuous improvementDirect all planning, scheduling, and production functions to ensure adequate materials, equipment, and personnel are available to meet the production scheduleEvaluate the functional strengths and developmental areas in the GMP manufacturing team and focuses on continuous improvement  qualifications: B.S. and/or M.S. in Biology, Biochemistry, Chemistry, Engineering or related field10+ years supervising an aseptic filling operationExperience with automatic filling equipmentAbility to work by influencing peers and their reports and gain their cooperationAbility to see the "big picture" while being capable of driving detailed, tactical execution. A high sense of urgency and a commitment to delivering results is essentialIntermediate proficiency in quality document systems, word processing, and spreadsheet packages  skills: Biology, Chemistry, 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: Watertown MA based company who provides novel solutions to clients for advanced therapy process development and manufacturing which is establishing the first end-to-end manufacturing capability for mRNA is actively seeking (1) Director of Drug Product Fill/Finish Manufacturing starting ASAP!! This is a full-time Permanent opportunity with flexible day shift hours, no weekends. The Director of Product Manufacturing will lead the establishment of the full Fill/Finish value chain for the company. This person is responsible for building, maintaining, and continuously improving a highly effective Fill/Finish capability including filling, visual inspection, labelling, and packaging operations for mRNA as well as a variety of sterile parenteral products using state-of-the-art equipment. They will provide the leadership, management, and vision necessary to ensure that the company has the proper controls, KPI, people, and systems in place within the Fill/Finish and manufacturing function. Great location which has numerous attractions including dozens of excellent shopping spots, restaurants, museums, historical sites, colleges and much more. Located of the Mass Pike and their are plenty of commuter rail stops for commuters!!   location: Watertown, Massachusetts job type: Permanent salary: $190,000 - 210,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Direct all day-to-day fill-finish manufacturing operating including but not limited to aseptic filling and product labeling and packaging to ensure delivery of departmental commitments to achieve company objectivesEstablish a Best-in-Class Fill/Finish value chain for the company and its clientsDevelop a robust visual inspection training program/strategyDirect all planning, scheduling, and production functions to ensure adequate materials, equipment, and personnel are available to meet the production scheduleEncourage and enforce a culture of compliance and continuous improvement regarding Safety and QualityDevelops and implements Key Performance Indicators to track and lead successful, timely achievement of goals, objectives, and projectsMaintains departmental operational and capital budget, responsible for driving financial results, drives optimization of fixed and variable costProvide leadership and direction to ensure Inspections, Deviations, Change Control, CAPAs and Regulatory commitments are met on time with the highest standards of qualityEvaluate the functional strengths and developmental areas in the GMP manufacturing team and focuses on continuous improvement.Must stay current with relevant technologies and forward thinking to identify new approachesDirect all day-to-day Fill and Finish manufacturing operations including but not limited to manufacturing, manufacturing support, & manufacturing compliance to ensure delivery of departmental commitments to achieve company objectivesDirect all planning, scheduling, and production functions to ensure adequate materials, equipment, and personnel are available to meet the production scheduleEvaluate the functional strengths and developmental areas in the GMP manufacturing team and focuses on continuous improvementDirect all planning, scheduling, and production functions to ensure adequate materials, equipment, and personnel are available to meet the production scheduleEvaluate the functional strengths and developmental areas in the GMP manufacturing team and focuses on continuous improvement  qualifications: B.S. and/or M.S. in Biology, Biochemistry, Chemistry, Engineering or related field10+ years supervising an aseptic filling operationExperience with automatic filling equipmentAbility to work by influencing peers and their reports and gain their cooperationAbility to see the "big picture" while being capable of driving detailed, tactical execution. A high sense of urgency and a commitment to delivering results is essentialIntermediate proficiency in quality document systems, word processing, and spreadsheet packages  skills: Biology, Chemistry, 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.
    • north wales, pennsylvania (remote)
    • permanent
    • $150,000 - $200,000 per year
    job summary: Exciting opportunity to join a world-class CRO as a senior/principal biostatistician, fully remote!   location: North Wales, Pennsylvania job type: Permanent salary: $150,000 - 200,000 per year work hours: 9 to 5 education: Masters   responsibilities: Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies.Serves as an independent reporting statistician on data monitoring committees.Develops statistical analysis plans and reporting specifications for simple to complex clinical studies.Reviews statistical analyses of other statisticians and interprets results from simple to complex clinical studies.Performs senior review of TFLs and statistical analysis plans.Provides significant input in the development and review of CRFs, edit specifications, and critical variable lists.  qualifications: Master's degree in statistics or biostatistics required. PhD preferred. Minimum of 6 years of biostatistical experience desired.Oncology experience preferredExhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices.Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials.  skills: Biostatistical Analysis 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: Exciting opportunity to join a world-class CRO as a senior/principal biostatistician, fully remote!   location: North Wales, Pennsylvania job type: Permanent salary: $150,000 - 200,000 per year work hours: 9 to 5 education: Masters   responsibilities: Serves as the lead biostatistician on programs of studies or submissions, or on simple to complex individual studies.Serves as an independent reporting statistician on data monitoring committees.Develops statistical analysis plans and reporting specifications for simple to complex clinical studies.Reviews statistical analyses of other statisticians and interprets results from simple to complex clinical studies.Performs senior review of TFLs and statistical analysis plans.Provides significant input in the development and review of CRFs, edit specifications, and critical variable lists.  qualifications: Master's degree in statistics or biostatistics required. PhD preferred. Minimum of 6 years of biostatistical experience desired.Oncology experience preferredExhibits expertise in multiple statistical areas, the drug development process, SAS procedures, and good programming practices.Demonstrates ability to plan, supervise, implement, and monitor the statistical processes for multiple clinical trials.  skills: Biostatistical Analysis 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.
    • novato, california
    • contract
    • $26 - $32.20 per hour
    job summary: Immediate needs for 20+ Biopharmaceutical Manufacturing Associates with a leading, global company located in the North Bay region of the Bay area. Shifts: All shifts available. 1st shift (7am-3pm), 2nd shift (3pm-11pm), and 3rd shift (11pm-7am). Positions may be 5x8 hour shift, 4x10 hour shift, 3x12 and 4x12 hour shift. Manufacturing operations are 24/7, so this requires multiple off shift coverage. Shifts will be discussed at time of interview. Position Type: 1 year contract, long term with potential for full time hire This role requires employees to be fully vaccinated against COVID-19   location: Novato, California job type: Contract salary: $26.00 - 32.20 per hour work hours: 9 to 5 education: Associate   responsibilities: Operate large scale bioprocess equipment for the Cell Culture and Purification operations.Prepare Buffer and Media solutions.Perform all aspects of processing: preparation of equipment, disassembling equipment, assembling process equipment, perform CIP and SIP of equipment, perform pressure tests of equipment, perform I Testing of filters, calibration and use of analytical equipment.Display competency with process equipment and automated control systemsKnowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.Proficiency with compliance; adherence to standard operating procedures, batch record, good documentation practices and data capturing WORK ENVIRONMENT/PHYSICAL DEMANDS Consists of strenuous, repetitive work. The following list of physical movements maybe used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands.Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds.May require work around loud equipment.The use of personal protective equipment will be required.Requires various shift based work and off hours  qualifications: Bachelor's degree (BS) in science related area or engineeringAssociate's degree (AS) in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industryStrong communication skills-verbal and writtenAbility to work in a team environment which includes good conflict resolution and collaborationDisplays good initiative to identify areas for improvement and implement solutions   skills: 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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: Immediate needs for 20+ Biopharmaceutical Manufacturing Associates with a leading, global company located in the North Bay region of the Bay area. Shifts: All shifts available. 1st shift (7am-3pm), 2nd shift (3pm-11pm), and 3rd shift (11pm-7am). Positions may be 5x8 hour shift, 4x10 hour shift, 3x12 and 4x12 hour shift. Manufacturing operations are 24/7, so this requires multiple off shift coverage. Shifts will be discussed at time of interview. Position Type: 1 year contract, long term with potential for full time hire This role requires employees to be fully vaccinated against COVID-19   location: Novato, California job type: Contract salary: $26.00 - 32.20 per hour work hours: 9 to 5 education: Associate   responsibilities: Operate large scale bioprocess equipment for the Cell Culture and Purification operations.Prepare Buffer and Media solutions.Perform all aspects of processing: preparation of equipment, disassembling equipment, assembling process equipment, perform CIP and SIP of equipment, perform pressure tests of equipment, perform I Testing of filters, calibration and use of analytical equipment.Display competency with process equipment and automated control systemsKnowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.Proficiency with compliance; adherence to standard operating procedures, batch record, good documentation practices and data capturing WORK ENVIRONMENT/PHYSICAL DEMANDS Consists of strenuous, repetitive work. The following list of physical movements maybe used on a daily basis: bending, reaching, climbing stairs and ladders, kneeling and making numerous equipment connections using hands.Independently have the ability to regularly lift, dispense, push and/or pull items with an average weight of 25 pounds.May require work around loud equipment.The use of personal protective equipment will be required.Requires various shift based work and off hours  qualifications: Bachelor's degree (BS) in science related area or engineeringAssociate's degree (AS) in science related area or Biotech certificate with 2+ years of experience in a biotech manufacturing environment or other regulated industryStrong communication skills-verbal and writtenAbility to work in a team environment which includes good conflict resolution and collaborationDisplays good initiative to identify areas for improvement and implement solutions   skills: 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • wyandotte, michigan
    • contract
    • $25 - $29.87 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Wyandotte, Michigan job type: Contract salary: $25.00 - 29.87 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Reviews GMP documentation (e.g., procedures, reports, methods, validation protocols, investigations, and corrective actions)Writes and reviews QA department procedures and reportsAssists with planning and conducting internal compliance auditsSupports supplier quality activities (qualification, risk management, and notification management)Participates in change control and CAPA implementation activitiesEnsures action plans are developed and completed in a timely fashionPrepares and review of site performance report, management review, and quality metricsImplementing continuous improvement projects (e.g., batch records, process data review)Other duties/projects, as assignedAdditional Requirements:Knowledge of quality/continuous improvement tools (SPC, Statistics, DOE, Six Sigma) preferredAbility to read technical literature and documents and extract important concepts.Good oral and written communication skills.Ability to write reports, data analysis, and business correspondenceAbility to convey project accomplishments, obstacles, issues and status clearly and concisely to team members.  qualifications: Bachelor's Degree, preferably in Science or Engineering, or equivalent related work experience is required Quality Assurance/Regulatory Affairs/Compliance experience is preferred   skills: Quality Assurance, CAPA, 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Wyandotte, Michigan job type: Contract salary: $25.00 - 29.87 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Reviews GMP documentation (e.g., procedures, reports, methods, validation protocols, investigations, and corrective actions)Writes and reviews QA department procedures and reportsAssists with planning and conducting internal compliance auditsSupports supplier quality activities (qualification, risk management, and notification management)Participates in change control and CAPA implementation activitiesEnsures action plans are developed and completed in a timely fashionPrepares and review of site performance report, management review, and quality metricsImplementing continuous improvement projects (e.g., batch records, process data review)Other duties/projects, as assignedAdditional Requirements:Knowledge of quality/continuous improvement tools (SPC, Statistics, DOE, Six Sigma) preferredAbility to read technical literature and documents and extract important concepts.Good oral and written communication skills.Ability to write reports, data analysis, and business correspondenceAbility to convey project accomplishments, obstacles, issues and status clearly and concisely to team members.  qualifications: Bachelor's Degree, preferably in Science or Engineering, or equivalent related work experience is required Quality Assurance/Regulatory Affairs/Compliance experience is preferred   skills: Quality Assurance, CAPA, 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.
    • marlborough, massachusetts
    • temporary
    • $20 - $28 per hour
    The HR Coordinator/ Administrative role for Randstad/Hologic is an integral part of the HR Shared Services team, whose goal it is to fulfill our employer promise through the development of enhanced experiences and signature moments. This role will be comprised of administrative and data entry job duties to support the HR team.  Role is located in Marlborough, MA and is a hybrid of remote and onsite. Onsite work will be 2-3 days a week and remote work is available 1-2 days a week. Schedule: 8am to 4:30pm Mon-Fri. salary: $20 - $28 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities• Will manage the daily transactions within the Oracle HCM system including answering questions & resolving issues • Perform any manual employee information changes in HCM System • Ensure data integrity, accuracy, and timeliness by conducting system audits of all electronic information • Prepare and maintain confidential HR documents, files, and other correspondence with respect to new hires, terminations, promotions, transfers, and other employee/department transactions • Establishes and maintains necessary record keeping and filing in compliance with federal, state and local laws • Work closely with HR Business Partners to provide any ad-hoc reporting to support the business • Respond to employment verifications and other general employee data/document requests.The essential functions of this role include:working in a smoke free environmentSkillsData EntryHRISPhonesOrganizational SkillsEditingMulti-taskingWritten CommunicationMicrosoft OfficeQualificationsYears of experience: 2 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.
    The HR Coordinator/ Administrative role for Randstad/Hologic is an integral part of the HR Shared Services team, whose goal it is to fulfill our employer promise through the development of enhanced experiences and signature moments. This role will be comprised of administrative and data entry job duties to support the HR team.  Role is located in Marlborough, MA and is a hybrid of remote and onsite. Onsite work will be 2-3 days a week and remote work is available 1-2 days a week. Schedule: 8am to 4:30pm Mon-Fri. salary: $20 - $28 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilities• Will manage the daily transactions within the Oracle HCM system including answering questions & resolving issues • Perform any manual employee information changes in HCM System • Ensure data integrity, accuracy, and timeliness by conducting system audits of all electronic information • Prepare and maintain confidential HR documents, files, and other correspondence with respect to new hires, terminations, promotions, transfers, and other employee/department transactions • Establishes and maintains necessary record keeping and filing in compliance with federal, state and local laws • Work closely with HR Business Partners to provide any ad-hoc reporting to support the business • Respond to employment verifications and other general employee data/document requests.The essential functions of this role include:working in a smoke free environmentSkillsData EntryHRISPhonesOrganizational SkillsEditingMulti-taskingWritten CommunicationMicrosoft OfficeQualificationsYears of experience: 2 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.
    • research triangle park, north carolina
    • contract
    • $21.83 - $24.92 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: Durham, North Carolina job type: Contract salary: $21.83 - 24.92 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Supporting the company's efforts to be the leader in neuroscience, this role plays a pivotal role in strengthening the company's reputation and leadership in Corporate Responsibility (CR). The role will help the company Community Lab in Cambridge, MA achieve its goal to excite more students about science by exposing them to authentic hands-on laboratory experiences and the variety of career opportunities in the biotech industry. This role will also assist in maintaining and growing the company's global community programs and engaging and inspiring employees. This role will be responsible for the day-to-day operations of the Cambridge Community Lab in Cambridge, MA including: coordinating scheduling and other logistical arrangements for student and teacher visits both local and global (virtual visits), ensuring that all protocols, reagents and materials are prepared for each class or program, recruiting employee volunteers, and most importantly, teaching the hands-on lab experiences to visiting middle and high school students. This role is also responsible for providing teacher professional development, developing and testing new curriculum pieces or other Community lab related projects, acting as a liaison with the local school districts and community groups and mentoring summer interns. Additionally, this role will be responsible for assisting with employee engagement programs such as volunteer efforts, employee matching gifts and museum benefits. Teach established hands-on lab experiences for middle and high school studentsMaintain an orderly Community Lab space and prepare, order and keep track of reagents and documents (set-up and clean-up)Communicate with teachers and community groups and actively maintain the booking calendarCreate communications to promote the company's community efforts (example: emails, newsletters, updates to intranet, maintain Community Lab page on their web page, and provide input on items for social media)Collect basic data on Community Lab usageCollaborate with external partners who assist with Community Lab programs, like Lemelson-MITCoordinate employee volunteersManage common email boxesWork cross-functionally with internal company groups to coordinate corporate responsibility programs (example: employee kid's events)Collaborate on opportunities to enhance the company's presence in the communityAssist with employee engagement programs (examples: volunteer efforts, employee matching gifts and local museum memberships)  qualifications: Bachelor's degree is required preferably in the life sciencesBackground in the biological sciences with demonstrated laboratory experience and strong understanding of the life sciences industry and key technologies and methods used in itStrong understanding of the education, nonprofit and community landscape in the Boston Metro areaPassionate and dynamic personalityEnthusiasm for working with middle and high school studentsTeam player and collaborative while able to lead independently and effectively prioritize workloadExcellent oral and presentation/teaching skills with preferred classroom/teaching experienceDemonstrated self-starter with excellent follow-through, attention to detail, organizational skills and high sense of urgencyCreative, pioneering, agile and flexible. Possesses a natural curiosity and enjoys working in a fast-paced environment  skills: Biology, 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. 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: Durham, North Carolina job type: Contract salary: $21.83 - 24.92 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Supporting the company's efforts to be the leader in neuroscience, this role plays a pivotal role in strengthening the company's reputation and leadership in Corporate Responsibility (CR). The role will help the company Community Lab in Cambridge, MA achieve its goal to excite more students about science by exposing them to authentic hands-on laboratory experiences and the variety of career opportunities in the biotech industry. This role will also assist in maintaining and growing the company's global community programs and engaging and inspiring employees. This role will be responsible for the day-to-day operations of the Cambridge Community Lab in Cambridge, MA including: coordinating scheduling and other logistical arrangements for student and teacher visits both local and global (virtual visits), ensuring that all protocols, reagents and materials are prepared for each class or program, recruiting employee volunteers, and most importantly, teaching the hands-on lab experiences to visiting middle and high school students. This role is also responsible for providing teacher professional development, developing and testing new curriculum pieces or other Community lab related projects, acting as a liaison with the local school districts and community groups and mentoring summer interns. Additionally, this role will be responsible for assisting with employee engagement programs such as volunteer efforts, employee matching gifts and museum benefits. Teach established hands-on lab experiences for middle and high school studentsMaintain an orderly Community Lab space and prepare, order and keep track of reagents and documents (set-up and clean-up)Communicate with teachers and community groups and actively maintain the booking calendarCreate communications to promote the company's community efforts (example: emails, newsletters, updates to intranet, maintain Community Lab page on their web page, and provide input on items for social media)Collect basic data on Community Lab usageCollaborate with external partners who assist with Community Lab programs, like Lemelson-MITCoordinate employee volunteersManage common email boxesWork cross-functionally with internal company groups to coordinate corporate responsibility programs (example: employee kid's events)Collaborate on opportunities to enhance the company's presence in the communityAssist with employee engagement programs (examples: volunteer efforts, employee matching gifts and local museum memberships)  qualifications: Bachelor's degree is required preferably in the life sciencesBackground in the biological sciences with demonstrated laboratory experience and strong understanding of the life sciences industry and key technologies and methods used in itStrong understanding of the education, nonprofit and community landscape in the Boston Metro areaPassionate and dynamic personalityEnthusiasm for working with middle and high school studentsTeam player and collaborative while able to lead independently and effectively prioritize workloadExcellent oral and presentation/teaching skills with preferred classroom/teaching experienceDemonstrated self-starter with excellent follow-through, attention to detail, organizational skills and high sense of urgencyCreative, pioneering, agile and flexible. Possesses a natural curiosity and enjoys working in a fast-paced environment  skills: Biology, 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.
    • nashville, tennessee
    • contract
    • $30 - $32 per hour
    job summary: Exciting opportunity to join a top-tier research center as a Clinical Research Coordinator!   location: Nashville, Tennessee job type: Contract salary: $30 - 32 per hour work hours: 9 to 5 education: Associate   responsibilities: Performs routine operational activities for multiple research protocolsLiaise between site research personnel, industry sponsors, and SupervisorCollaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicableCoordinates schedule of assessments from initial submission of feasibility until study closeoutReviews the study design and inclusion/exclusion criteria with physician and patientEnsures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements  qualifications: Effective communication skillsStrong organizational skills and time managementBasic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping  skills: Clinical research 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: Exciting opportunity to join a top-tier research center as a Clinical Research Coordinator!   location: Nashville, Tennessee job type: Contract salary: $30 - 32 per hour work hours: 9 to 5 education: Associate   responsibilities: Performs routine operational activities for multiple research protocolsLiaise between site research personnel, industry sponsors, and SupervisorCollaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicableCoordinates schedule of assessments from initial submission of feasibility until study closeoutReviews the study design and inclusion/exclusion criteria with physician and patientEnsures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements  qualifications: Effective communication skillsStrong organizational skills and time managementBasic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping  skills: Clinical research 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.
    • los angeles, california
    • contract
    • $30 - $35 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: Los Angeles, California job type: Contract salary: $30 - 35 per hour work hours: 3 to 11 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. Perform environmental monitoring of clean rooms and controlled areas to support qualifications and routine sampling of the facility and critical utilities including WFI, compressed gas, nitrogen, etc. Conduct microbial-based assays including bioburden testing, microbial quantification, and organism identification. Additional testing includes LAL, pH, TOC, and Conductivity.Perform review of test data with application of GDP.Will be required to perform change requests (e.g. ECR, DCR) when required and complete them in a timely manner. Assure SOPs are updated; prepare and update as determined.Identification and issuance of Alert/OOL forms for out of limit results. May be required to conduct investigations into Alert/OOL excursions.Investigate deviations and write exception documents as required, utilizing problem-solving tools as needed.Support execution of validations for lab equipment, lab methods, or facility projects.May be required to generate, execute, and summarize special laboratory studies.  qualifications: Good project management skills a plus.  skills: Laboratory Information Management Systems (LIMS), 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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: Los Angeles, California job type: Contract salary: $30 - 35 per hour work hours: 3 to 11 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. Perform environmental monitoring of clean rooms and controlled areas to support qualifications and routine sampling of the facility and critical utilities including WFI, compressed gas, nitrogen, etc. Conduct microbial-based assays including bioburden testing, microbial quantification, and organism identification. Additional testing includes LAL, pH, TOC, and Conductivity.Perform review of test data with application of GDP.Will be required to perform change requests (e.g. ECR, DCR) when required and complete them in a timely manner. Assure SOPs are updated; prepare and update as determined.Identification and issuance of Alert/OOL forms for out of limit results. May be required to conduct investigations into Alert/OOL excursions.Investigate deviations and write exception documents as required, utilizing problem-solving tools as needed.Support execution of validations for lab equipment, lab methods, or facility projects.May be required to generate, execute, and summarize special laboratory studies.  qualifications: Good project management skills a plus.  skills: Laboratory Information Management Systems (LIMS), 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • somerville, new jersey
    • contract
    • $35 - $40.66 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Somerville, New Jersey job type: Contract salary: $35.00 - 40.66 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Conduct laboratory experiments to generate reliable and consistent data in a timely manner.Document, discuss, and modify experimental studies as needed in collaboration with other team members and/or project lead.Summarize data and assist project lead in maintaining project documentation.  qualifications: Bachelor degree in mechanical engineering, material science, biomedical engineering or a related field with 1+ years of academic or industry laboratory experienceExperience with performing and troubleshooting a wide variety of material characterization assays is desiredDemonstrated ability to quickly learn new concepts, skills and techniquesCapable of contributing independently but also work successfully in a highly collaborative scientific environmentPossess strong written and oral communication skillsWorking knowledge of MS Office (Excel, Word, PowerPoint) and basic understanding of statistical analyses is a plusMeticulous attention to detail and diligence in record keeping  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Biology, GLP (Good Laboratory Practice), 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Somerville, New Jersey job type: Contract salary: $35.00 - 40.66 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Conduct laboratory experiments to generate reliable and consistent data in a timely manner.Document, discuss, and modify experimental studies as needed in collaboration with other team members and/or project lead.Summarize data and assist project lead in maintaining project documentation.  qualifications: Bachelor degree in mechanical engineering, material science, biomedical engineering or a related field with 1+ years of academic or industry laboratory experienceExperience with performing and troubleshooting a wide variety of material characterization assays is desiredDemonstrated ability to quickly learn new concepts, skills and techniquesCapable of contributing independently but also work successfully in a highly collaborative scientific environmentPossess strong written and oral communication skillsWorking knowledge of MS Office (Excel, Word, PowerPoint) and basic understanding of statistical analyses is a plusMeticulous attention to detail and diligence in record keeping  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Biology, GLP (Good Laboratory Practice), 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.
    • worcester, massachusetts
    • contract
    • $25 - $30.43 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Worcester, Massachusetts job type: Contract salary: $25.00 - 30.43 per hour work hours: 7 to 3 education: Bachelors   responsibilities: Performs test methods as written to support product/material release.Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirementsWill perform a multitude of laboratory techniques for which they are trainedAccepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectives.Revises procedures as necessary and provides support for department.Support investigationsWill effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.  qualifications: Bachelors Degree or Advanced Degree in a Biotechnology related science, or completion of Biotechnology Certificate programPrevious GMP, and/or Lab Experience within a Pharmaceutical, Biotechnology, Medical, or Medical Technology environment.  skills: Quality control, MS-WORD, MS-EXCEL, GLP (Good Laboratory Practice), 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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: Worcester, Massachusetts job type: Contract salary: $25.00 - 30.43 per hour work hours: 7 to 3 education: Bachelors   responsibilities: Performs test methods as written to support product/material release.Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirementsWill perform a multitude of laboratory techniques for which they are trainedAccepts responsibility to complete assigned tasks as committed. Works with others to maintain a positive atmosphere to accomplish business objectives.Revises procedures as necessary and provides support for department.Support investigationsWill effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.  qualifications: Bachelors Degree or Advanced Degree in a Biotechnology related science, or completion of Biotechnology Certificate programPrevious GMP, and/or Lab Experience within a Pharmaceutical, Biotechnology, Medical, or Medical Technology environment.  skills: Quality control, MS-WORD, MS-EXCEL, GLP (Good Laboratory Practice), 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.
    • delaware, ohio
    • contract
    • $20.50 - $21 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 11 to 7 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 11 to 7 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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.
    • delaware, ohio
    • contract
    • $20.50 - $21 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 7 to 3 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 7 to 3 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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.
    • delaware, ohio
    • contract
    • $20.50 - $21 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 11 to 7 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 11 to 7 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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.
    • delaware, ohio
    • contract
    • $20.50 - $21 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 3 to 11 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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: Delaware, Ohio job type: Contract salary: $20.50 - 21.00 per hour work hours: 3 to 11 education: High School   responsibilities: Quality Control Lab Technician, Entry Job Description ?As a Quality Control Lab Technician, you will be responsible primarily for testing samples that come from production! The testing includes basic wet testing (viscosity, density, total non-volatiles) and paint application using various application tools, including hand spray and machine spray methods. Technicians will be required to detail the results of their testing. Are you self-motivated? You will have the opportunity to evaluate prepared panels for color, gloss, and appearance! Ultimately, you will be encouraged to evaluate test results, adjust batches based on physical and color properties, and approve batches for the customer. Key Responsibilities: Working safely by following all safety rules, and wearing appropriate PPE Participating in group lab tasks, maintaining stock levels and cleanliness of lab Accurate testing of production samples Following procedures and work direction Applying paint to test panels Evaluating application quality and adjusting application parameters Clear documentation of test results Gaining basic understanding of products and specifications Gaining ability to understand and react to test results   qualifications: Required - high school diploma, strong work history, or college experience. Required - ability to work overtime, including Saturdays and/or Sundays. Preferred - College degree in any field. Experience in lab environment.  skills: 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.
    • buena park, california
    • permanent
    • $110,000 - $120,000 per year
    job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a Sr. Regulatory professional in the Los Angeles, CA area. The ideal candidate will be apart of the Nutrition Regulatory Affairs & Safety team functions as a progressive global group that ensures product compliance and safety in every step of the product lifecycle. This group delivers scientifically sound regulatory strategies, which provide our Business Owners (ABO's) confidence, that they are selling a superior product. On this team you will provide counsel to cross functional teams on ingredient acceptability, formulation design, product labeling, claims and registration requirements. Working with our global team, we also monitor and interpret the impact of current, pending, and future regulations to ensure the Nutrition portfolio maintains compliance. If you would enjoy working on a technical, global, cross functional team, this is a terrific opportunity to showcase your skills! This is a direct hire opportunity and can start immediately.   location: Buena Park, California job type: Permanent salary: $110,000 - 120,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: What's special about this team: The Nutrition Regulatory Affairs & Safety team functions as a progressive global group that ensures product compliance and safety in every step of the product lifecycle. This group delivers scientifically sound regulatory strategies, which provide our Business Owners (ABO's) confidence, that they are selling a superior product. On this team you will provide counsel to cross functional teams on ingredient acceptability, formulation design, product labeling, claims and registration requirements. Working with our global team, we also monitor and interpret the impact of current, pending, and future regulations to ensure the Nutrition portfolio maintains compliance. If you would enjoy working on a technical, global, cross functional team, this is a terrific opportunity to showcase your skills! How you would contribute to the role: In this role, you will be a key team member to lead the regulatory activities of product design, ensuring successful regulatory pathways for nutrition products sold in over 80 countries and territories around the globe. By partnering with key stakeholders both in our corporate environment, and around the world, your ability to guide nutrition product development teams and bring regulatory compliant solutions for innovative product design challenges, will be of great value. You will lead concept, ingredient, formula, and finished product assessments, international label and claims development, for new nutrition products. Additionally, you will have the opportunity to work with our global team, developing relationships with regulatory partners both internally, and in the industry. This role involves executing regulatory strategies in a dynamic product development setting to enable product access across the globe. If you enjoy work with a strategic focus, that offers global collaboration, this role may be for you!   qualifications: What skills and background will be important to be successful: Minimum 6 years scientific background (Regulatory, Science, Health/Nutrition, International Affairs or related degree) with use of analytical and scientific databasesKnowledge of global food/nutrition regulations, communicating and interpreting regulatory challengesExperience leading cross functional global project teams successfully through risk management scenariosA solution-oriented mindset, providing strategic regulatory recommendations for improvementsTalent to communicate across cultures, with the ability to influence stakeholdersRAPS certification desirable, or experience with food/nutrition laws and/or requirementsBS degree in Food, Regulatory Science, or a related sciences discipline (MS degree preferred) *This position is NOT eligible for sponsorship*   skills: CMC, FDA, HACCP, Biology, Chemistry, Regulatory Affairs Operations, Regulatory Affairs Strategy, Regulatory Briefing Documents, Submissions, Food Product Development 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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: Randstad is the #1 HR Services Company in the world and we are sourcing for a Sr. Regulatory professional in the Los Angeles, CA area. The ideal candidate will be apart of the Nutrition Regulatory Affairs & Safety team functions as a progressive global group that ensures product compliance and safety in every step of the product lifecycle. This group delivers scientifically sound regulatory strategies, which provide our Business Owners (ABO's) confidence, that they are selling a superior product. On this team you will provide counsel to cross functional teams on ingredient acceptability, formulation design, product labeling, claims and registration requirements. Working with our global team, we also monitor and interpret the impact of current, pending, and future regulations to ensure the Nutrition portfolio maintains compliance. If you would enjoy working on a technical, global, cross functional team, this is a terrific opportunity to showcase your skills! This is a direct hire opportunity and can start immediately.   location: Buena Park, California job type: Permanent salary: $110,000 - 120,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: What's special about this team: The Nutrition Regulatory Affairs & Safety team functions as a progressive global group that ensures product compliance and safety in every step of the product lifecycle. This group delivers scientifically sound regulatory strategies, which provide our Business Owners (ABO's) confidence, that they are selling a superior product. On this team you will provide counsel to cross functional teams on ingredient acceptability, formulation design, product labeling, claims and registration requirements. Working with our global team, we also monitor and interpret the impact of current, pending, and future regulations to ensure the Nutrition portfolio maintains compliance. If you would enjoy working on a technical, global, cross functional team, this is a terrific opportunity to showcase your skills! How you would contribute to the role: In this role, you will be a key team member to lead the regulatory activities of product design, ensuring successful regulatory pathways for nutrition products sold in over 80 countries and territories around the globe. By partnering with key stakeholders both in our corporate environment, and around the world, your ability to guide nutrition product development teams and bring regulatory compliant solutions for innovative product design challenges, will be of great value. You will lead concept, ingredient, formula, and finished product assessments, international label and claims development, for new nutrition products. Additionally, you will have the opportunity to work with our global team, developing relationships with regulatory partners both internally, and in the industry. This role involves executing regulatory strategies in a dynamic product development setting to enable product access across the globe. If you enjoy work with a strategic focus, that offers global collaboration, this role may be for you!   qualifications: What skills and background will be important to be successful: Minimum 6 years scientific background (Regulatory, Science, Health/Nutrition, International Affairs or related degree) with use of analytical and scientific databasesKnowledge of global food/nutrition regulations, communicating and interpreting regulatory challengesExperience leading cross functional global project teams successfully through risk management scenariosA solution-oriented mindset, providing strategic regulatory recommendations for improvementsTalent to communicate across cultures, with the ability to influence stakeholdersRAPS certification desirable, or experience with food/nutrition laws and/or requirementsBS degree in Food, Regulatory Science, or a related sciences discipline (MS degree preferred) *This position is NOT eligible for sponsorship*   skills: CMC, FDA, HACCP, Biology, Chemistry, Regulatory Affairs Operations, Regulatory Affairs Strategy, Regulatory Briefing Documents, Submissions, Food Product Development 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • newbury park, california
    • contract
    • $25 - $29.08 per hour
    job summary: This role is responsible for performing the day-to-day quality operations. You will identify and assess quality risks in activities and processes according to regulatory agency rules, guidelines, and Takeda quality practices. Schedule/Shift: 1st shift, Mon.-Fri., 8am-4:30pm Position Type: Contract position for 6 mos. with potential for extension. 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: Newbury Park, California job type: Contract salary: $25.00 - 29.08 per hour work hours: 8 to 4 education: High School   responsibilities: Review pertinent documents, against Standard Operating Procedures (SOPs) for accuracy and compliance based on regulatory requirements and internal guidelines, etc.Identify areas of nonconformance and escalate to management (Manufacturing and Quality) for initiation of a Deviation.Conduct, perform, and/or review investigations for non-conformances within respective area. Assist in identifying corrective actions to prevent recurring non-conformances.Administer and maintain relevant databases, prepare, and issue reports defined by the area, and develop custom reports as needed.Assist in external and internal audits/inspections by maintaining audit records, extracting data from databases, and creating reports, collecting relevant data, etc.Support process with timely closure of observations/audit items.Serve as a team member and/or assist in CAPA Investigations for significant issues within respective area.Maintain and update departmental business indicators.Prepare metrics for the Management Review of Quality Systems.Audit/review documents as needed for completeness, CGMP's, company procedures and verification of data. Correct any deficiencies found.Assist and/or prepare Annual Product Review (APR) for products as directed.Write Technical reports (e.g., PQR and YBPR)Assist in the development, review, and revision of SOPs in support of Division Procedure Compliance and continuous improvement efforts as needed.Assist in training Quality team membersMay perform other duties as assigned  qualifications: High school diploma or equivalent required .Bachelor's degree (BS) in a scientific discipline preferred .Three (3) to five (5) years of related work experience.The overall physical exertion of this position is sedentary.May require lifting and carrying of up to 10 lbs.Batch record Review on the Floor (BRR) may require being on your feet for long periods of time.Strong interpersonal skills and great attention to detail are necessary.Strong team player with effective communication skills and able to handle multiple projects concurrentlyAble to apply problem solving tools and methods to coordinate and/or lead investigation teams.Good understanding of Current Good Manufacturing Practices (CGMP) as well as Good Documentation Practices (GDP).Knowledge of FDA regulations, Application of Good Laboratory Practices and Application of Good Manufacturing PracticesExperience with Microsoft Excel, Word, and PowerPointNormal office environment.Able to work in controlled or clean room environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body. No make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in these work environments.May work in a cold, wet environment or cool/hot storage conditions; may be exposed to sunlight, heat, dust, gases and fumesMay climb up and into large processing tanks for cleaning or inspection.May be working in a loud area that requires hearing protection and other protective equipment to be worn.May work around chemicals such as alcohol, acids, buffers and celite that may require respiratory protection.May be required to work in a confined area as defined by the Environmental, Health, & Safety office.May be required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes.May require immunization before performing work within the manufacturing area.May require overtime, weekend, and holiday work.May be assigned to a different shift as needed.  skills: FDA, Quality Assurance, MS-WORD, CAPA, MS-EXCEL, MS-Powerpoint, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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 is responsible for performing the day-to-day quality operations. You will identify and assess quality risks in activities and processes according to regulatory agency rules, guidelines, and Takeda quality practices. Schedule/Shift: 1st shift, Mon.-Fri., 8am-4:30pm Position Type: Contract position for 6 mos. with potential for extension. 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: Newbury Park, California job type: Contract salary: $25.00 - 29.08 per hour work hours: 8 to 4 education: High School   responsibilities: Review pertinent documents, against Standard Operating Procedures (SOPs) for accuracy and compliance based on regulatory requirements and internal guidelines, etc.Identify areas of nonconformance and escalate to management (Manufacturing and Quality) for initiation of a Deviation.Conduct, perform, and/or review investigations for non-conformances within respective area. Assist in identifying corrective actions to prevent recurring non-conformances.Administer and maintain relevant databases, prepare, and issue reports defined by the area, and develop custom reports as needed.Assist in external and internal audits/inspections by maintaining audit records, extracting data from databases, and creating reports, collecting relevant data, etc.Support process with timely closure of observations/audit items.Serve as a team member and/or assist in CAPA Investigations for significant issues within respective area.Maintain and update departmental business indicators.Prepare metrics for the Management Review of Quality Systems.Audit/review documents as needed for completeness, CGMP's, company procedures and verification of data. Correct any deficiencies found.Assist and/or prepare Annual Product Review (APR) for products as directed.Write Technical reports (e.g., PQR and YBPR)Assist in the development, review, and revision of SOPs in support of Division Procedure Compliance and continuous improvement efforts as needed.Assist in training Quality team membersMay perform other duties as assigned  qualifications: High school diploma or equivalent required .Bachelor's degree (BS) in a scientific discipline preferred .Three (3) to five (5) years of related work experience.The overall physical exertion of this position is sedentary.May require lifting and carrying of up to 10 lbs.Batch record Review on the Floor (BRR) may require being on your feet for long periods of time.Strong interpersonal skills and great attention to detail are necessary.Strong team player with effective communication skills and able to handle multiple projects concurrentlyAble to apply problem solving tools and methods to coordinate and/or lead investigation teams.Good understanding of Current Good Manufacturing Practices (CGMP) as well as Good Documentation Practices (GDP).Knowledge of FDA regulations, Application of Good Laboratory Practices and Application of Good Manufacturing PracticesExperience with Microsoft Excel, Word, and PowerPointNormal office environment.Able to work in controlled or clean room environments requiring special gowning. Will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet, and body. No make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in these work environments.May work in a cold, wet environment or cool/hot storage conditions; may be exposed to sunlight, heat, dust, gases and fumesMay climb up and into large processing tanks for cleaning or inspection.May be working in a loud area that requires hearing protection and other protective equipment to be worn.May work around chemicals such as alcohol, acids, buffers and celite that may require respiratory protection.May be required to work in a confined area as defined by the Environmental, Health, & Safety office.May be required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes.May require immunization before performing work within the manufacturing area.May require overtime, weekend, and holiday work.May be assigned to a different shift as needed.  skills: FDA, Quality Assurance, MS-WORD, CAPA, MS-EXCEL, MS-Powerpoint, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • newbury park, california
    • contract
    • $41 - $44 per hour
    job summary: The Quality Specialist role is responsible for review of Deviations, Protocols, Change Controls and Risk assessments within the Quality Release team. Schedule/Shift: 1st shift, Mon.-Fri., 8am-4:30pm. Position Type: Contract position for 6 mos. with potential for extension. 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: Newbury Park, California job type: Contract salary: $41 - 44 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for review of quality related documentation and approval of events and change control including assessing the risk and impact to the process and/or product as applicable.Write professional reports (PQRs), analyze data and identify and assess quality risk in activities and processes according to guidelines and company standard operating procedures.Initiate document change proposals, prepare/review/approve protocols to justify process changes, approve validation protocols, and assist with training and auditing as appropriate.Lead ongoing daily departmental activities for areas of direct responsibility and when required assist other Quality areas in the successful performance of these activities.Write Product Annual Review Reports for multiple productsResponsible for overseeing the closure of nonconformance reports pertaining to areas of responsibility. Able to apply problem solving tools and methods to coordinate and/or lead investigation teams. Lead investigations (i.e. CAPA) for process failures within respective areas.Responsible for trending and analyzing data, and presentation of Quality System indicators to all organizational levels.Acts as a change-agent and drives continuous improvement activities within the QA Formulation and Filling organization and across the facility as assigned.Proactively participates in processes and serves as a driver for general process/system improvements.May perform other duties as assigned.General knowledge of manufacturing processes, laboratory operations, and/or critical systems preferred.Strong verbal, written and oral communication skills.Good interpersonal/communication/influencing/negotiation skills.Good project management skills.Proficient in Microsoft Word, Excel and Data Analysis and project management.Ability to perform technical writing of reports. Able to proofread and reconcile data for accuracy.  qualifications: Bachelor's degree (BS) in Science or Engineering preferred.Minimum of five (5) - eight (8) years of experience in quality operations or related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.  skills: SOP, Quality Assurance, MS-WORD, CAPA, MS-EXCEL 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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 Specialist role is responsible for review of Deviations, Protocols, Change Controls and Risk assessments within the Quality Release team. Schedule/Shift: 1st shift, Mon.-Fri., 8am-4:30pm. Position Type: Contract position for 6 mos. with potential for extension. 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: Newbury Park, California job type: Contract salary: $41 - 44 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for review of quality related documentation and approval of events and change control including assessing the risk and impact to the process and/or product as applicable.Write professional reports (PQRs), analyze data and identify and assess quality risk in activities and processes according to guidelines and company standard operating procedures.Initiate document change proposals, prepare/review/approve protocols to justify process changes, approve validation protocols, and assist with training and auditing as appropriate.Lead ongoing daily departmental activities for areas of direct responsibility and when required assist other Quality areas in the successful performance of these activities.Write Product Annual Review Reports for multiple productsResponsible for overseeing the closure of nonconformance reports pertaining to areas of responsibility. Able to apply problem solving tools and methods to coordinate and/or lead investigation teams. Lead investigations (i.e. CAPA) for process failures within respective areas.Responsible for trending and analyzing data, and presentation of Quality System indicators to all organizational levels.Acts as a change-agent and drives continuous improvement activities within the QA Formulation and Filling organization and across the facility as assigned.Proactively participates in processes and serves as a driver for general process/system improvements.May perform other duties as assigned.General knowledge of manufacturing processes, laboratory operations, and/or critical systems preferred.Strong verbal, written and oral communication skills.Good interpersonal/communication/influencing/negotiation skills.Good project management skills.Proficient in Microsoft Word, Excel and Data Analysis and project management.Ability to perform technical writing of reports. Able to proofread and reconcile data for accuracy.  qualifications: Bachelor's degree (BS) in Science or Engineering preferred.Minimum of five (5) - eight (8) years of experience in quality operations or related field within a biotechnology, biologics, or pharmaceutical manufacturing facility.  skills: SOP, Quality Assurance, MS-WORD, CAPA, MS-EXCEL 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • los angeles, california
    • contract
    • $25.84 - $30.39 per hour
    job summary: This role will be leading lab investigations and overseeing CAPA records in Trackwise. There is a lot of data gathering and must be efficient on the computer. Schedule/Shift: 1st shift, Mon.-Fri., 8am-4:30pm Position Type: Contract position for 6 mos. w/ potential for extension. 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: Los Angeles, California job type: Contract salary: $25.84 - 30.39 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The primary responsibility of this role is to manage lab investigations and CAPA records in Trackwise.Role requires performing administrative duties such as collecting lab data, completing investigation records, filing timely extensions and progressing records through the action and effectiveness phases.Must be able to manage multiple records at once.Must be comfortable communicating with different departments to get updates on action items.Able to follow general writing template and receive feedback.Opportunity to develop and/or implement sustainable tracking system to manage records.Other responsibilities may include trending, data compilation, and other similar tasks as assigned.  qualifications: Must have strong organizational skillsMust have solid writing skillsMust have strong attention to detailTrackwise experience requiredPharmaceutical with laboratory background preferred***There is a lot of data gathering and must be efficient on the computer.***  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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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 will be leading lab investigations and overseeing CAPA records in Trackwise. There is a lot of data gathering and must be efficient on the computer. Schedule/Shift: 1st shift, Mon.-Fri., 8am-4:30pm Position Type: Contract position for 6 mos. w/ potential for extension. 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: Los Angeles, California job type: Contract salary: $25.84 - 30.39 per hour work hours: 9 to 5 education: No Degree Required   responsibilities: The primary responsibility of this role is to manage lab investigations and CAPA records in Trackwise.Role requires performing administrative duties such as collecting lab data, completing investigation records, filing timely extensions and progressing records through the action and effectiveness phases.Must be able to manage multiple records at once.Must be comfortable communicating with different departments to get updates on action items.Able to follow general writing template and receive feedback.Opportunity to develop and/or implement sustainable tracking system to manage records.Other responsibilities may include trending, data compilation, and other similar tasks as assigned.  qualifications: Must have strong organizational skillsMust have solid writing skillsMust have strong attention to detailTrackwise experience requiredPharmaceutical with laboratory background preferred***There is a lot of data gathering and must be efficient on the computer.***  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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • myerstown, pennsylvania
    • temporary
    • $42 - $44 per hour
    Randstad is seeking an experienced Data Analyst to develop and deploy sustainable databases, dashboards and solutions while working with Production, IT & data teams to support decision making, generating KPIs and reliability for our client's business. Our client is a global life sciences company, focused in healthcare and pharmaceutical research.Requirements: Degree in all Engineers, Statistics, Informatics, Data Science, Computational or related discipline. Experience in Data Analytics and reports.Proficiency in computational skills, desired experience building automated data science workflowsProficiency in Data visualizationCommunication competencies to include presentations, concise and actionable manner to broad audiences and key stakeholders across multiple functionsAbility to influence key stakeholders through challenges and opportunities salary: $42 - $44 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesProvide technical contributions in a fast-paced team environment to accelerate efforts on building analytics-driven solutions. • Work within the analytics community, partners in regional areas to present structured and unstructured data from different sources, clean and validate the data to ensure accuracy, completeness, and uniformity. • Assess the needs of automation in data, implement and sustainable automation solutions. • Develop sustainable, consumable, accurate, and impactful data reporting solutions. • Compile data from internal and external sources and construct data-driven decision-making processes. • Utilize available data sets and data science best practices to identify business risks and opportunities. Activity influences procedures and/or company policy. • Seek and build collaborations among teams to have the most accurate data.Skills Data Analytics (2 years of experience is required)Statistics (2 years of experience is required)Data Visualization (2 years of experience is required) Qualifications Years of experience: 2 yearsExperience level: Experienced Randstad 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.
    Randstad is seeking an experienced Data Analyst to develop and deploy sustainable databases, dashboards and solutions while working with Production, IT & data teams to support decision making, generating KPIs and reliability for our client's business. Our client is a global life sciences company, focused in healthcare and pharmaceutical research.Requirements: Degree in all Engineers, Statistics, Informatics, Data Science, Computational or related discipline. Experience in Data Analytics and reports.Proficiency in computational skills, desired experience building automated data science workflowsProficiency in Data visualizationCommunication competencies to include presentations, concise and actionable manner to broad audiences and key stakeholders across multiple functionsAbility to influence key stakeholders through challenges and opportunities salary: $42 - $44 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesProvide technical contributions in a fast-paced team environment to accelerate efforts on building analytics-driven solutions. • Work within the analytics community, partners in regional areas to present structured and unstructured data from different sources, clean and validate the data to ensure accuracy, completeness, and uniformity. • Assess the needs of automation in data, implement and sustainable automation solutions. • Develop sustainable, consumable, accurate, and impactful data reporting solutions. • Compile data from internal and external sources and construct data-driven decision-making processes. • Utilize available data sets and data science best practices to identify business risks and opportunities. Activity influences procedures and/or company policy. • Seek and build collaborations among teams to have the most accurate data.Skills Data Analytics (2 years of experience is required)Statistics (2 years of experience is required)Data Visualization (2 years of experience is required) Qualifications Years of experience: 2 yearsExperience level: Experienced Randstad 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.
    • libertyville, illinois
    • contract
    • $22 - $23.50 per hour
    job summary: Coordinator - Quality Control Sample - 2 OPENINGS 1st shift - M-F (8-430pm) Duties The Coordinator, Quality Control Sample, provides sample control support at a Manufacturing facility.   location: Libertyville, Illinois job type: Contract salary: $22.00 - 23.50 per hour work hours: 8 to 4 education: Associate   responsibilities: Responsibilities: Create sample tracking and inventory system to track development samplesAdministration of QC in-process, release, and stability samples, associated document coordination, and collection of data. Additional responsibilities include Adherence to all GMP requirements, a basic understanding of FDA/EMEA regulations, effective interactions/communication with Quality management, personal development, and support of investigations.May support the Manager for activities related to training of employees, compliance with GMP, and identifying and implementing corrective and preventive actions.Generate sample submission forms for various testing facilitiesCollect sample forecasts to ensure lead time noticeConfirm testing was complete when sample invoices arriveFollow/track international shipments, and alert logistics group of any customs clearance issuesInspect incoming sample shipments and take necessary actions if samples do not comply with SOPsReview and evaluate temperature data reports from temperature monitoring devices included with sample shipmentsCreate equipment, inventory, and sample receipt and tracking logbooksDraft sample management proceduresCommunicate with other departments including Quality Assurance, Manufacturing and Facilities to address compliance issues and to implement corrective actions and to improve programs.Write and revise documents such as SOPs and technical reports.Other related duties as assigned. Requirements: Associates Degree in scientific field and 2 years of related experience in a GMP Quality Control laboratory.B.A. or B.S. in microbiology or related scientific field preferred.Excellent oral and written communication skills with strong technical writing experience required.Possess an understanding of the requirements of Sample Coordination in a GMP laboratory.Ability to work effectively within the group, within Quality, and across the site.  qualifications: Requirements: Associates Degree in scientific field and 2 years of related experience in a GMP Quality Control laboratory.B.A. or B.S. in microbiology or related scientific field preferred.Excellent oral and written communication skills with strong technical writing experience required.Possess an understanding of the requirements of Sample Coordination in a GMP laboratory.Ability to work effectively within the group, within Quality, and across the site.  skills: 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: Coordinator - Quality Control Sample - 2 OPENINGS 1st shift - M-F (8-430pm) Duties The Coordinator, Quality Control Sample, provides sample control support at a Manufacturing facility.   location: Libertyville, Illinois job type: Contract salary: $22.00 - 23.50 per hour work hours: 8 to 4 education: Associate   responsibilities: Responsibilities: Create sample tracking and inventory system to track development samplesAdministration of QC in-process, release, and stability samples, associated document coordination, and collection of data. Additional responsibilities include Adherence to all GMP requirements, a basic understanding of FDA/EMEA regulations, effective interactions/communication with Quality management, personal development, and support of investigations.May support the Manager for activities related to training of employees, compliance with GMP, and identifying and implementing corrective and preventive actions.Generate sample submission forms for various testing facilitiesCollect sample forecasts to ensure lead time noticeConfirm testing was complete when sample invoices arriveFollow/track international shipments, and alert logistics group of any customs clearance issuesInspect incoming sample shipments and take necessary actions if samples do not comply with SOPsReview and evaluate temperature data reports from temperature monitoring devices included with sample shipmentsCreate equipment, inventory, and sample receipt and tracking logbooksDraft sample management proceduresCommunicate with other departments including Quality Assurance, Manufacturing and Facilities to address compliance issues and to implement corrective actions and to improve programs.Write and revise documents such as SOPs and technical reports.Other related duties as assigned. Requirements: Associates Degree in scientific field and 2 years of related experience in a GMP Quality Control laboratory.B.A. or B.S. in microbiology or related scientific field preferred.Excellent oral and written communication skills with strong technical writing experience required.Possess an understanding of the requirements of Sample Coordination in a GMP laboratory.Ability to work effectively within the group, within Quality, and across the site.  qualifications: Requirements: Associates Degree in scientific field and 2 years of related experience in a GMP Quality Control laboratory.B.A. or B.S. in microbiology or related scientific field preferred.Excellent oral and written communication skills with strong technical writing experience required.Possess an understanding of the requirements of Sample Coordination in a GMP laboratory.Ability to work effectively within the group, within Quality, and across the site.  skills: 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.
    • north chicago, illinois
    • contract
    • $30 - $35.40 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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 Chicago, Illinois job type: Contract salary: $30.00 - 35.40 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Regulatory Affairs Analyst, reviews, and assess incoming global regulatory information for entry into Company's registration and documentation management systems.Interacts with all areas of regulatory affairs and affiliates to ensure registration management information is current, accurate and available in regulatory systems.Executes established business processes and may assist in development and implementation of process/system changes and/or data remediation projects. Troubleshoots errors and system performance issues and works with supervisor and IT on business problem resolution and enhancements.Participates and contributes to group, department, and cross-functional meetings.May also assist in training junior team members.  qualifications: Bachelor's Degree, 4+ years in a related area including manufacturing, regulatory affairs, R&D, or quality in the pharmaceutical, medical device, or other healthcare industry.Experience/understanding/use of software tools.Demonstrated analytical and communication skills.Skills and knowledge of drug submissions  skills: IND, FDA, MS-WORD, MS-EXCEL, 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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is 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 Chicago, Illinois job type: Contract salary: $30.00 - 35.40 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Regulatory Affairs Analyst, reviews, and assess incoming global regulatory information for entry into Company's registration and documentation management systems.Interacts with all areas of regulatory affairs and affiliates to ensure registration management information is current, accurate and available in regulatory systems.Executes established business processes and may assist in development and implementation of process/system changes and/or data remediation projects. Troubleshoots errors and system performance issues and works with supervisor and IT on business problem resolution and enhancements.Participates and contributes to group, department, and cross-functional meetings.May also assist in training junior team members.  qualifications: Bachelor's Degree, 4+ years in a related area including manufacturing, regulatory affairs, R&D, or quality in the pharmaceutical, medical device, or other healthcare industry.Experience/understanding/use of software tools.Demonstrated analytical and communication skills.Skills and knowledge of drug submissions  skills: IND, FDA, MS-WORD, MS-EXCEL, 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.
    • cambridge, massachusetts (remote)
    • contract
    • $103.09 - $114.54 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: $103.09 - 114.54 per hour work hours: 9 to 5 education: Bachelors   responsibilities: