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18 jobs found in worcester, massachusetts

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    • worcester, massachusetts
    • contract
    • $40 - $48.13 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: $40.00 - 48.13 per hour work hours: 9 to 5 education: Masters   responsibilities: Design, optimize, and execute high content cellular imaging assays using genomic manipulations techniques, small or large molecules to study cellular trafficking and pathway biology Practical experience with designing and executing cellular assays on high content imaging platforms, data analysis and visualizationExcellent computer skills and a good understanding of basic image analysis software Experienced with working with 2D and 3D in-vitro model systems Experienced with low and HTS screening methodsExperience with designing Co-Culture model systems Experienced with liquid handling automation systemsExperienced with trouble shooting in-vitro assays and validating in-vitro assays Experienced with protocol write-ups Experienced with corelating target modulation with phenotype while screening or characterizing large or small moleculesWork collaboratively with project teams to deliver targets across portfolioDemonstrate scientific excellence, work ethic, and dedication to team and project goalsWork collaboratively in a matrix with project teams and members of the Biologics Group to drive innovation and deliver novel therapies to patientsDevelop productive collaborations and communication with other groups across therapeutic areas  qualifications: MS in related discipline 3 -5 years industry/lab experience High Content Imaging (Florescent Microscopy, Cellular Staining, Imaging analysis etc.)  skills: PCR, Biology 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: $40.00 - 48.13 per hour work hours: 9 to 5 education: Masters   responsibilities: Design, optimize, and execute high content cellular imaging assays using genomic manipulations techniques, small or large molecules to study cellular trafficking and pathway biology Practical experience with designing and executing cellular assays on high content imaging platforms, data analysis and visualizationExcellent computer skills and a good understanding of basic image analysis software Experienced with working with 2D and 3D in-vitro model systems Experienced with low and HTS screening methodsExperience with designing Co-Culture model systems Experienced with liquid handling automation systemsExperienced with trouble shooting in-vitro assays and validating in-vitro assays Experienced with protocol write-ups Experienced with corelating target modulation with phenotype while screening or characterizing large or small moleculesWork collaboratively with project teams to deliver targets across portfolioDemonstrate scientific excellence, work ethic, and dedication to team and project goalsWork collaboratively in a matrix with project teams and members of the Biologics Group to drive innovation and deliver novel therapies to patientsDevelop productive collaborations and communication with other groups across therapeutic areas  qualifications: MS in related discipline 3 -5 years industry/lab experience High Content Imaging (Florescent Microscopy, Cellular Staining, Imaging analysis etc.)  skills: PCR, Biology 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 - $29.04 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 - 29.04 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Execute high through put scale down robotic purification from early stage to late stage for cross function groups, viral clearance, process characterization, and continuous process improvement studies, performing basic data acquisition and analysis, documenting in electric lab notebooksWill develop economical, robust steps for recovering the target protein from bioreactor harvests using chromatography, filtration, and other separation techniques; developing downstream purification processes to be transferred to Manufacturing; and performing laboratory scale process characterization studies.The individual can perform various bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.The candidate must possess strong written, oral, and collaborative skills in order to effectively communicate experimental procedures and results.As appropriate, the candidate may supply technical support for pilot and/or GMP manufacturing of clinical materials.  qualifications: 0 to 5 years of experience, Bachelor's degree bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.  skills: HPLC, Biology 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 - 29.04 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Execute high through put scale down robotic purification from early stage to late stage for cross function groups, viral clearance, process characterization, and continuous process improvement studies, performing basic data acquisition and analysis, documenting in electric lab notebooksWill develop economical, robust steps for recovering the target protein from bioreactor harvests using chromatography, filtration, and other separation techniques; developing downstream purification processes to be transferred to Manufacturing; and performing laboratory scale process characterization studies.The individual can perform various bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.The candidate must possess strong written, oral, and collaborative skills in order to effectively communicate experimental procedures and results.As appropriate, the candidate may supply technical support for pilot and/or GMP manufacturing of clinical materials.  qualifications: 0 to 5 years of experience, Bachelor's degree bioanalytical assays, including HPLC, ELISAs and SDS-PAGE, to aid in rapid process development.  skills: HPLC, Biology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $35 - $39.28 per hour
    job summary: The Quality Assurance (QA) Operations department is responsible for quality oversight of operations at company's Framingham Biologics facilities. QA's main responsibility is to ensure adherence to CGMPs during manufacturing operations through partnership with the site and direct engagement with daily operations activities. Quality Assurance Operations is responsible for providing support and guidance to the Company Operations function in order to protect the safety, quality and efficacy of company's products, thereby ensuring the availability of compliant and safe products for our patients and assuring the security of the company's business and global markets. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $35.00 - 39.28 per hour work hours: 7 to 3 education: Bachelors   responsibilities: The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team.Actively supports the QA Operations team by providing technical supportCompletes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change ControlsEnsure all safety requirements are being metPerforms batch record and logbook reviewPerforms review of column packing and qualification recordsReview and approve CRs related to EBRsFunction as SME on challenges related to production requiring quality inputProvide on the floor (OTF) support to the operations department, including OTF support for critical operations stepsIssue action notices and conduct affiliated provisional releaseConduct log book audits against compliance requirementsReview CV related documentation against specificationPerform media / buffer and intermediate releasePerform release of Cell Banks for forward processing (as applicable)Support cross-functional internal audit activities and conduct walkthrough inspectionsExecute containment activitiesProvide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRsMaintain a high level of personal compliance to the required standardsPartner with manufacturing and support operations to ensure a culture of continuous compliance  qualifications: Basic Qualifications: Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field.Knowledge in external agency regulations (FDA, EMA, etc.)Strong computer, verbal and written communication skills.Experience in quality systems.Experience with Trackwise or equivalent system.Proficient in Microsoft Office Preferred Qualifications: Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation.Experience with company Manufacturing System (SMS) or comparable continuous improvement systems.Experience with root cause analysis tools.Demonstrated experience with change control, CAPA and deviation quality systems.Experience in a Quality Assurance role.Strong technical writing skills.Effective time management, attention to detail, organizational skills, teamwork and collaboration.Significant capability in problem solving methodology.Experience training and technically developing employees.Experience participating in external agency inspections.Knowledge of regulatory enforcement trends.Ability to work independently Special Working Conditions: Ability to gown and gain entry to manufacturing and Quality Control areas.Ability to work a 12-hour rotating shift and every other weekend, including holidays.Ability to lift 10 lbs.  skills: MS-WORD, CAPA, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Quality Assurance (QA) Operations department is responsible for quality oversight of operations at company's Framingham Biologics facilities. QA's main responsibility is to ensure adherence to CGMPs during manufacturing operations through partnership with the site and direct engagement with daily operations activities. Quality Assurance Operations is responsible for providing support and guidance to the Company Operations function in order to protect the safety, quality and efficacy of company's products, thereby ensuring the availability of compliant and safe products for our patients and assuring the security of the company's business and global markets. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $35.00 - 39.28 per hour work hours: 7 to 3 education: Bachelors   responsibilities: The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team.Actively supports the QA Operations team by providing technical supportCompletes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change ControlsEnsure all safety requirements are being metPerforms batch record and logbook reviewPerforms review of column packing and qualification recordsReview and approve CRs related to EBRsFunction as SME on challenges related to production requiring quality inputProvide on the floor (OTF) support to the operations department, including OTF support for critical operations stepsIssue action notices and conduct affiliated provisional releaseConduct log book audits against compliance requirementsReview CV related documentation against specificationPerform media / buffer and intermediate releasePerform release of Cell Banks for forward processing (as applicable)Support cross-functional internal audit activities and conduct walkthrough inspectionsExecute containment activitiesProvide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRsMaintain a high level of personal compliance to the required standardsPartner with manufacturing and support operations to ensure a culture of continuous compliance  qualifications: Basic Qualifications: Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field.Knowledge in external agency regulations (FDA, EMA, etc.)Strong computer, verbal and written communication skills.Experience in quality systems.Experience with Trackwise or equivalent system.Proficient in Microsoft Office Preferred Qualifications: Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation.Experience with company Manufacturing System (SMS) or comparable continuous improvement systems.Experience with root cause analysis tools.Demonstrated experience with change control, CAPA and deviation quality systems.Experience in a Quality Assurance role.Strong technical writing skills.Effective time management, attention to detail, organizational skills, teamwork and collaboration.Significant capability in problem solving methodology.Experience training and technically developing employees.Experience participating in external agency inspections.Knowledge of regulatory enforcement trends.Ability to work independently Special Working Conditions: Ability to gown and gain entry to manufacturing and Quality Control areas.Ability to work a 12-hour rotating shift and every other weekend, including holidays.Ability to lift 10 lbs.  skills: MS-WORD, CAPA, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • worcester, massachusetts
    • contract
    • $25 - $31.53 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 - 31.53 per hour work hours: 9 to 5 education: Bachelors   responsibilities: In vivo skills, especially on mice.Sampling, profiling, and processing of tissue samples for downstream applications in a timely manner. Tissue homogenizing, qRT-PCR, ELISA, MSD.Familiarity with statistical and research methodologyAbility to work both independently as well as within project teams  qualifications: BS or MS in dermatology, immunology, biology, or related field with a minimum of 3 years hand-on in vivo experience.  skills: Biology, Immunoassays, In Vivo 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 - 31.53 per hour work hours: 9 to 5 education: Bachelors   responsibilities: In vivo skills, especially on mice.Sampling, profiling, and processing of tissue samples for downstream applications in a timely manner. Tissue homogenizing, qRT-PCR, ELISA, MSD.Familiarity with statistical and research methodologyAbility to work both independently as well as within project teams  qualifications: BS or MS in dermatology, immunology, biology, or related field with a minimum of 3 years hand-on in vivo experience.  skills: Biology, Immunoassays, In Vivo 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
    • $40 - $48.13 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: $40.00 - 48.13 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform routine sample preparation including cells, tissue, and biological fluid, and perform assay execution to support LC/MS proteomics studies related to disease MOA, target identification and biomarker discoveryLearn new methods and assays to process quantity-limited samples to support single-cell and spatial proteomics studiesMaintain laboratory equipment, stock basic laboratory supplies and chemicals, lab logistics inducing sample shipping and receiving, and coordinate waste removal as needed.Maintain a clear, detailed laboratory notebook to document all experiments and findings  qualifications: BS, MS or PhD degree in analytical science, chemistry, biochemistry, biology, or related technical discipline with typically 3+ (MS), or 0+ (PhD) years of relevant experience. Experience in biotech/pharmaceutical industry setting or academic core lab is preferred.Minimum 2+ years of laboratory experience.Strong problem-solving skills and the ability to work independently or with minimum supervision.Work well both independently and as part of a teamPassion to learn new skillset in a fast-paced environment  skills: HPLC, MS-WORD, MS-EXCEL, Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory 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: $40.00 - 48.13 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform routine sample preparation including cells, tissue, and biological fluid, and perform assay execution to support LC/MS proteomics studies related to disease MOA, target identification and biomarker discoveryLearn new methods and assays to process quantity-limited samples to support single-cell and spatial proteomics studiesMaintain laboratory equipment, stock basic laboratory supplies and chemicals, lab logistics inducing sample shipping and receiving, and coordinate waste removal as needed.Maintain a clear, detailed laboratory notebook to document all experiments and findings  qualifications: BS, MS or PhD degree in analytical science, chemistry, biochemistry, biology, or related technical discipline with typically 3+ (MS), or 0+ (PhD) years of relevant experience. Experience in biotech/pharmaceutical industry setting or academic core lab is preferred.Minimum 2+ years of laboratory experience.Strong problem-solving skills and the ability to work independently or with minimum supervision.Work well both independently and as part of a teamPassion to learn new skillset in a fast-paced environment  skills: HPLC, MS-WORD, MS-EXCEL, Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory 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.
    • framingham, massachusetts
    • contract
    • $22 - $27.67 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $22.00 - 27.67 per hour work hours: 8 to 4 education: Bachelors   responsibilities: ? Ensures the efficiency of Quality System implemented between company and the sub- contractors ensuring a relevant management for complaints, deviations, change controls, non-conformities or any activity aiming to ensure the production, the control and the release of products accordingly with Quality requirements. ? Leads projects as assigned such as new product launch teams. ? Identify and leads the resolution of quality related issues that impact cGMP compliance, regulatory filings, or other risks, to company products. ? Collaborates with subcontractors to find and implement solutions concerning quality issues. ? Respond to customer complaints, including close out and determination of corrective actions by collaborating with CMO's and identifying trends. ? Identify and prevent or resolve issues that could impact the continuity of supply of existing products. ? Review/Approve sub-contractor's validation protocols, Master Documents and significant deviations and investigations. Identify trends to reduce Quality anomalies. ? Constant contact with the Senior Director of Quality and Regulatory, EM- North America and Global Quality. Knowledge/Competencies ? Excellent oral and written communication skills in cGMP documentation. ? Experience in 3rd party manufacturing Quality and Regulatory function and/or same plant experience ? Interpersonal skills to interface with suppliers and customer to develop privileged communications and relationship ? The incumbent should possess significant technical knowledge related to typical Quality Assurance activities in the pharmaceutical and medical device industries especially those related to handling product complaints and the associated regulations ? Understanding of various drug product manufacturing including oral dosages, semi-solids, liquids, injectables, lyophilized and medical drug/device combinations ? Project management skills   qualifications: ? Bachelor of Science ? 5-7 years in Pharmaceutical Operations or Quality Operations with the application of cGMPs in the Pharmaceutical or related regulated industry   skills: MS-WORD, 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. 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $22.00 - 27.67 per hour work hours: 8 to 4 education: Bachelors   responsibilities: ? Ensures the efficiency of Quality System implemented between company and the sub- contractors ensuring a relevant management for complaints, deviations, change controls, non-conformities or any activity aiming to ensure the production, the control and the release of products accordingly with Quality requirements. ? Leads projects as assigned such as new product launch teams. ? Identify and leads the resolution of quality related issues that impact cGMP compliance, regulatory filings, or other risks, to company products. ? Collaborates with subcontractors to find and implement solutions concerning quality issues. ? Respond to customer complaints, including close out and determination of corrective actions by collaborating with CMO's and identifying trends. ? Identify and prevent or resolve issues that could impact the continuity of supply of existing products. ? Review/Approve sub-contractor's validation protocols, Master Documents and significant deviations and investigations. Identify trends to reduce Quality anomalies. ? Constant contact with the Senior Director of Quality and Regulatory, EM- North America and Global Quality. Knowledge/Competencies ? Excellent oral and written communication skills in cGMP documentation. ? Experience in 3rd party manufacturing Quality and Regulatory function and/or same plant experience ? Interpersonal skills to interface with suppliers and customer to develop privileged communications and relationship ? The incumbent should possess significant technical knowledge related to typical Quality Assurance activities in the pharmaceutical and medical device industries especially those related to handling product complaints and the associated regulations ? Understanding of various drug product manufacturing including oral dosages, semi-solids, liquids, injectables, lyophilized and medical drug/device combinations ? Project management skills   qualifications: ? Bachelor of Science ? 5-7 years in Pharmaceutical Operations or Quality Operations with the application of cGMPs in the Pharmaceutical or related regulated industry   skills: MS-WORD, 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. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $30 - $35.71 per hour
    job summary: Quality Control Microbiology (QCM) is responsible for testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations.Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation.Quality Control is also responsible for assisting in site wide studies and projects.This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $30.00 - 35.71 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Perform laboratory assays in support of method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.Perform maintenance on complex laboratory equipment.Review data for compliance to procedures and specifications.Calculate and evaluate results.Make detailed observations in support of Alert, Action and OOS result investigations.Participate in writing and revising SOPs.Assists in the qualification of new controls, standards and reagentsEffectively demonstrate an understanding of and work in compliance with CGMPs.Practice safe work habits and adhere to Genzyme's safety procedures and guidelines.Actively participate in problem solving meetings with senior staff members and suggest process improvements.Independently work under supervision and direction.  qualifications: Leadership Qualifications: An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all of our products and services. This includes:Being a Subject Matter Expert (SME)/Trainer/Coach to other analysts within the laboratory.Constantly striving to make Genzyme a great place to work, and a company respected for the quality of its people and products.Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs. Basic Qualifications:Bachelor's degree or equivalent and 2 + years laboratory experience.Master's degree or equivalent and 0-1 year experience.Basic knowledge (i.e. 1-2 years experience) in the required method platform (e.g. Bioburden, TOC, Endotoxin, Water Chemistry, ELISA).Attention to detail, and able to maintain accurate records with excellent proofreading skillsAble to communicate effectively with othersAble to work effectively both independently and as a member of a teamProficient with Microsoft Office tools such as: Word, Excel & Powerpoint. Preferred Qualifications:Experience in GMP lab environment.Experience with lab based data management systems.Experience in a quality control lab. Special Working Conditions:Work in a laboratory with minimal use of chemicals.Ability to lift 10 lbs.  skills: MS-WORD, 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. 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: Quality Control Microbiology (QCM) is responsible for testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations.Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation.Quality Control is also responsible for assisting in site wide studies and projects.This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $30.00 - 35.71 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Perform laboratory assays in support of method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.Perform maintenance on complex laboratory equipment.Review data for compliance to procedures and specifications.Calculate and evaluate results.Make detailed observations in support of Alert, Action and OOS result investigations.Participate in writing and revising SOPs.Assists in the qualification of new controls, standards and reagentsEffectively demonstrate an understanding of and work in compliance with CGMPs.Practice safe work habits and adhere to Genzyme's safety procedures and guidelines.Actively participate in problem solving meetings with senior staff members and suggest process improvements.Independently work under supervision and direction.  qualifications: Leadership Qualifications: An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all of our products and services. This includes:Being a Subject Matter Expert (SME)/Trainer/Coach to other analysts within the laboratory.Constantly striving to make Genzyme a great place to work, and a company respected for the quality of its people and products.Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs. Basic Qualifications:Bachelor's degree or equivalent and 2 + years laboratory experience.Master's degree or equivalent and 0-1 year experience.Basic knowledge (i.e. 1-2 years experience) in the required method platform (e.g. Bioburden, TOC, Endotoxin, Water Chemistry, ELISA).Attention to detail, and able to maintain accurate records with excellent proofreading skillsAble to communicate effectively with othersAble to work effectively both independently and as a member of a teamProficient with Microsoft Office tools such as: Word, Excel & Powerpoint. Preferred Qualifications:Experience in GMP lab environment.Experience with lab based data management systems.Experience in a quality control lab. Special Working Conditions:Work in a laboratory with minimal use of chemicals.Ability to lift 10 lbs.  skills: MS-WORD, 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. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $38 - $41.42 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $38.00 - 41.42 per hour work hours: 7 to 3 education: Bachelors   responsibilities: The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team. - Actively supports the QA Operations team by providing technical support - Completes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change Controls - Ensure all safety requirements are being met - Performs batch record and logbook review - Performs review of column packing and qualification records - Review and approve CRs related to EBRs - Function as SME on challenges related to production requiring quality input - Provide on the floor (OTF) support to the operations department, including OTF support for critical operations steps - Issue action notices and conduct affiliated provisional release - Conduct log book audits against compliance requirements - Review CV related documentation against specification - Perform media / buffer and intermediate release - Perform release of Cell Banks for forward processing (as applicable) - Support cross-functional internal audit activities and conduct walkthrough inspections - Execute containment activities - Provide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRs - Maintain a high level of personal compliance to the required standards - Partner with manufacturing and support operations to ensure a culture of continuous compliance   qualifications: Basic Qualifications: - Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field. - Knowledge in external agency regulations (FDA, EMA, etc.) - Strong computer, verbal and written communication skills. - Experience in quality systems. - Experience with Trackwise or equivalent system. - Proficient in Microsoft Office Preferred Qualifications: - Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation. - Experience with company Manufacturing System (SMS) or comparable continuous improvement systems. - Experience with root cause analysis tools. - Demonstrated experience with change control, CAPA and deviation quality systems. - Experience in a Quality Assurance role. - Strong technical writing skills. - Effective time management, attention to detail, organizational skills, teamwork and collaboration. - Significant capability in problem solving methodology. - Experience training and technically developing employees. - Experience participating in external agency inspections. - Knowledge of regulatory enforcement trends. - Ability to work independently Special Working Conditions: - Ability to gown and gain entry to manufacturing and Quality Control areas. - Ability to lift 10 lbs.   skills: SOP, 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. 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $38.00 - 41.42 per hour work hours: 7 to 3 education: Bachelors   responsibilities: The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team. - Actively supports the QA Operations team by providing technical support - Completes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change Controls - Ensure all safety requirements are being met - Performs batch record and logbook review - Performs review of column packing and qualification records - Review and approve CRs related to EBRs - Function as SME on challenges related to production requiring quality input - Provide on the floor (OTF) support to the operations department, including OTF support for critical operations steps - Issue action notices and conduct affiliated provisional release - Conduct log book audits against compliance requirements - Review CV related documentation against specification - Perform media / buffer and intermediate release - Perform release of Cell Banks for forward processing (as applicable) - Support cross-functional internal audit activities and conduct walkthrough inspections - Execute containment activities - Provide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRs - Maintain a high level of personal compliance to the required standards - Partner with manufacturing and support operations to ensure a culture of continuous compliance   qualifications: Basic Qualifications: - Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field. - Knowledge in external agency regulations (FDA, EMA, etc.) - Strong computer, verbal and written communication skills. - Experience in quality systems. - Experience with Trackwise or equivalent system. - Proficient in Microsoft Office Preferred Qualifications: - Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation. - Experience with company Manufacturing System (SMS) or comparable continuous improvement systems. - Experience with root cause analysis tools. - Demonstrated experience with change control, CAPA and deviation quality systems. - Experience in a Quality Assurance role. - Strong technical writing skills. - Effective time management, attention to detail, organizational skills, teamwork and collaboration. - Significant capability in problem solving methodology. - Experience training and technically developing employees. - Experience participating in external agency inspections. - Knowledge of regulatory enforcement trends. - Ability to work independently Special Working Conditions: - Ability to gown and gain entry to manufacturing and Quality Control areas. - Ability to lift 10 lbs.   skills: SOP, 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. 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
    • $28 - $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: $28.00 - 30.43 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Performs test methods validations for clinical and commercial projects.Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.Performs a multitude of laboratory techniques for which they are trained.Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives.Authors validation protocols and reports as well as corresponding test methods.Support laboratory investigations in a timely manner.Support a variety of testing techniques upon completion of training.  qualifications: BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience.CE-SDS, HPLC or ELISA existing experience and troubleshooting experienceEmpower or Softmax / PLA software experience  skills: Quality control, HPLC, Phase iii, Chemistry, 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: $28.00 - 30.43 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Performs test methods validations for clinical and commercial projects.Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.Performs a multitude of laboratory techniques for which they are trained.Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives.Authors validation protocols and reports as well as corresponding test methods.Support laboratory investigations in a timely manner.Support a variety of testing techniques upon completion of training.  qualifications: BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience.CE-SDS, HPLC or ELISA existing experience and troubleshooting experienceEmpower or Softmax / PLA software experience  skills: Quality control, HPLC, Phase iii, Chemistry, 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
    • $30 - $33.54 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: $30.00 - 33.54 per hour work hours: 9 to 5 education: Masters   responsibilities: We are searching for a highly motivated Chemist III/IV to join with our Protein Analytics team at Company Bioresearch Center in Worcester, MA. Our team is responsible for the development, qualification, and execution of analytical methods to provide product and process understanding for biological entities from discovery through commercial stages.As a Chemist III/IV, you will be a part of the Analytical Characterization Group (ACG) within the Protein Analytics Department. ACG focuses on providing routine, investigative, and in-depth characterization analyses of Companys biologics to support product and process development for early-phase, late-phase, and commercial programs using liquid chromatography mass spectrometry (LC-MS), spectroscopy, and various other biophysical assays.The successful candidate will contribute to the development and performance of analytical assays and will contribute to the continuous improvement and innovation within ACG and the Protein Analytics Department.  qualifications: Working knowledge and hands-on experience with the following instrumentation: HPLC/UPLC and Mass Spectrometry. Strong documentation skills (for electronic laboratory notebook record keeping), laboratory bench skills (for sample preparation), and communication skills (for discussing/presenting results). Good fundamental understanding of biopharmaceuticals (such as proteins, monoclonal antibodies, etc.) and analytical/biophysical characterization techniques.  skills: HPLC, MS-WORD, MS-EXCEL, GLP (Good Laboratory 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: $30.00 - 33.54 per hour work hours: 9 to 5 education: Masters   responsibilities: We are searching for a highly motivated Chemist III/IV to join with our Protein Analytics team at Company Bioresearch Center in Worcester, MA. Our team is responsible for the development, qualification, and execution of analytical methods to provide product and process understanding for biological entities from discovery through commercial stages.As a Chemist III/IV, you will be a part of the Analytical Characterization Group (ACG) within the Protein Analytics Department. ACG focuses on providing routine, investigative, and in-depth characterization analyses of Companys biologics to support product and process development for early-phase, late-phase, and commercial programs using liquid chromatography mass spectrometry (LC-MS), spectroscopy, and various other biophysical assays.The successful candidate will contribute to the development and performance of analytical assays and will contribute to the continuous improvement and innovation within ACG and the Protein Analytics Department.  qualifications: Working knowledge and hands-on experience with the following instrumentation: HPLC/UPLC and Mass Spectrometry. Strong documentation skills (for electronic laboratory notebook record keeping), laboratory bench skills (for sample preparation), and communication skills (for discussing/presenting results). Good fundamental understanding of biopharmaceuticals (such as proteins, monoclonal antibodies, etc.) and analytical/biophysical characterization techniques.  skills: HPLC, MS-WORD, MS-EXCEL, GLP (Good Laboratory 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
    • $30 - $37.20 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: $30.00 - 37.20 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Design workflow, procedures and experiments in consultation with supervisor.Characterize antibodies by cell-based assays, ELISA, IP, Co-IP, Western Blot, and FACS.Maintain cell cultures including cell lines and primary cells.Maintain accurate and timely records of research and project activity in electronic notebookPerform routine tasks competently and independently and generate reliable and consistent results.Analyze and critique results, noting significant deviations; communicate the results clearly and timely with supervisor and team membersLearn and understand new experimental techniques.Demonstrate skills in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.Impact projects predominantly through lab-based activities.Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.   qualifications: Bachelors, Master's, or PhDs Degree with typically 3-5+ (BS) or 1-2+ (MS), or 0-1+ (PhD) years of experienceTheoretical and practical knowledge to carry out job functionExperienced in mammalian cell culture, cell-based assays such as reporter gene-based assays, immunocytochemistry, flow cytometry, and biochemical assays such as ELISA, immunoprecipitation and Western Blotting.Experience in protein purification is a plus.Strong communication and organization skills, especially the ability to work across multiple scientific disciplines and functionsAbility to perform productively and efficiently within a dynamic work environment.Knowledge and experience in biologics drug discovery is a plus.  skills: GLP (Good Laboratory Practice), Immunoassays, Flow Cytometry, Cell Cultures, 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: $30.00 - 37.20 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Design workflow, procedures and experiments in consultation with supervisor.Characterize antibodies by cell-based assays, ELISA, IP, Co-IP, Western Blot, and FACS.Maintain cell cultures including cell lines and primary cells.Maintain accurate and timely records of research and project activity in electronic notebookPerform routine tasks competently and independently and generate reliable and consistent results.Analyze and critique results, noting significant deviations; communicate the results clearly and timely with supervisor and team membersLearn and understand new experimental techniques.Demonstrate skills in multiple techniques and appropriately modify protocols, as required, to suit the changing needs of research or development sciences.Impact projects predominantly through lab-based activities.Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.   qualifications: Bachelors, Master's, or PhDs Degree with typically 3-5+ (BS) or 1-2+ (MS), or 0-1+ (PhD) years of experienceTheoretical and practical knowledge to carry out job functionExperienced in mammalian cell culture, cell-based assays such as reporter gene-based assays, immunocytochemistry, flow cytometry, and biochemical assays such as ELISA, immunoprecipitation and Western Blotting.Experience in protein purification is a plus.Strong communication and organization skills, especially the ability to work across multiple scientific disciplines and functionsAbility to perform productively and efficiently within a dynamic work environment.Knowledge and experience in biologics drug discovery is a plus.  skills: GLP (Good Laboratory Practice), Immunoassays, Flow Cytometry, Cell Cultures, 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
    • $20 - $26.48 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: $20.00 - 26.48 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Conduct investigations on internal nonconformance and customer complaints related to Reagents.Assist in developing/ improving Reagent manufacturing processes and/or products. Design experiments and testing schemes, analyze data, write protocols and reports and present results to a cross-functional team.  qualifications: Must demonstrate strong problem solving and analytical skills and be a team player.Must possess a BS in molecular biology, biochemistry, or related field with at least one to two years of relevant experience.Knowledge of GMP, ISO, and FDA regulations and audits a plus.Familiar with process and test method validations.Excellent communication skills.Shall be able to perform under pressure to meet project deadlines.  skills: Molecular Biology, Cell Biology, Flow Cytometry, Cell Cultures, 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: $20.00 - 26.48 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Conduct investigations on internal nonconformance and customer complaints related to Reagents.Assist in developing/ improving Reagent manufacturing processes and/or products. Design experiments and testing schemes, analyze data, write protocols and reports and present results to a cross-functional team.  qualifications: Must demonstrate strong problem solving and analytical skills and be a team player.Must possess a BS in molecular biology, biochemistry, or related field with at least one to two years of relevant experience.Knowledge of GMP, ISO, and FDA regulations and audits a plus.Familiar with process and test method validations.Excellent communication skills.Shall be able to perform under pressure to meet project deadlines.  skills: Molecular Biology, Cell Biology, Flow Cytometry, Cell Cultures, 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.
    • framingham, massachusetts
    • contract
    • $38 - $42.85 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $38.00 - 42.85 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Compliance Specialist II duties will include but not be limited to: Perform all aspects of batch record issuance, batch record review and lot release process, ensuring compliance to the relevant site release SOP and corporate standard.Perform review of product testing results in support of release of intermediates and finished goods.Perform final inspection of in process and finished goods.Participate in investigation of all lot-associated deviations, change controls (CCR), BuildingManagement System (BMS) and Environmental Management System (EMS) investigations, action notices and environmental excursions as required.Perform QA presence on the floor (oversight or AQL, as appropriate).Perform various Quality Management System (QMS) trending/reporting functions.Perform and/or participate in monthly compliance walkthroughs and review status of pest control logs.  qualifications: BachelorsYears' of experience 3-6Ability to lift 15lbs required to perform inspections  skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $38.00 - 42.85 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Compliance Specialist II duties will include but not be limited to: Perform all aspects of batch record issuance, batch record review and lot release process, ensuring compliance to the relevant site release SOP and corporate standard.Perform review of product testing results in support of release of intermediates and finished goods.Perform final inspection of in process and finished goods.Participate in investigation of all lot-associated deviations, change controls (CCR), BuildingManagement System (BMS) and Environmental Management System (EMS) investigations, action notices and environmental excursions as required.Perform QA presence on the floor (oversight or AQL, as appropriate).Perform various Quality Management System (QMS) trending/reporting functions.Perform and/or participate in monthly compliance walkthroughs and review status of pest control logs.  qualifications: BachelorsYears' of experience 3-6Ability to lift 15lbs required to perform inspections  skills: SOP Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $25 - $28.57 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $25.00 - 28.57 per hour work hours: 9 to 5 education: High School   responsibilities: Responsibilities include: - Data entry and filing of laboratory documentation - Request, maintain and return of logbooks used in the Quality Control Sample management. - Performing sample receipt and sample disposal in the Quality Control laboratory - Coordinates distribution of samples to other laboratories - Ordering of laboratory supplies - Manages laboratory reserve samples - Cleaning and storage of the laboratory glassware Effectively demonstrates an understanding of CGMPs and how it applies to specific responsibilities - Following accurate oral and written procedures for maintenance of laboratory systems, documentation, and samples - Ensures laboratory data and samples are effectively maintained - Updates laboratory database and tracks the completion of various functions required by the Quality Control laboratory - Works independently under general supervision and direction - Work in compliance with CGMPs - Practices safe work habits and adheres to safety procedures and guidelines   qualifications: Basic Qualifications - High school diploma/GED and 2 years' experience in a pharmaceutical environment - Proficient in Outlook, MS Word, Excel, and lab-based data management systems Preferred Qualifications - Associates Degree and 1 year experience in administrative setting OR - Bachelor's Degree - LMS experience - CGMP experience Special Working conditions - Must be able to lift 40 lbs. - Must be able to work with Spor-klenz solution, which is used to sanitize equipment following SOP guidelines. - Position is considered essential personnel and may be required to staff the lab during inclement weather events   skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $25.00 - 28.57 per hour work hours: 9 to 5 education: High School   responsibilities: Responsibilities include: - Data entry and filing of laboratory documentation - Request, maintain and return of logbooks used in the Quality Control Sample management. - Performing sample receipt and sample disposal in the Quality Control laboratory - Coordinates distribution of samples to other laboratories - Ordering of laboratory supplies - Manages laboratory reserve samples - Cleaning and storage of the laboratory glassware Effectively demonstrates an understanding of CGMPs and how it applies to specific responsibilities - Following accurate oral and written procedures for maintenance of laboratory systems, documentation, and samples - Ensures laboratory data and samples are effectively maintained - Updates laboratory database and tracks the completion of various functions required by the Quality Control laboratory - Works independently under general supervision and direction - Work in compliance with CGMPs - Practices safe work habits and adheres to safety procedures and guidelines   qualifications: Basic Qualifications - High school diploma/GED and 2 years' experience in a pharmaceutical environment - Proficient in Outlook, MS Word, Excel, and lab-based data management systems Preferred Qualifications - Associates Degree and 1 year experience in administrative setting OR - Bachelor's Degree - LMS experience - CGMP experience Special Working conditions - Must be able to lift 40 lbs. - Must be able to work with Spor-klenz solution, which is used to sanitize equipment following SOP guidelines. - Position is considered essential personnel and may be required to staff the lab during inclement weather events   skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $40 - $45.77 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $40.00 - 45.77 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for the execution and analysis of experiments and analytical procedures.Display an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures.Investigate basic technical problems and performs routine scientific procedures and experiments under general supervision.Plan and prioritize concurrent experimental procedures. Integrate, compile, and tabulate data and assist supervisor in the analysis and interpretation of the results.May provide oral presentations on results to other department members.Work under active supervision.Follow established procedures.Work is reviewed for soundness of technical judgment and overall adequacy and accuracy.Contribute to the completion of milestones associated with specific projects. Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources.Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters.  qualifications: Years of Experience: 6 - 9 YearsThis role requires execution of several assays. However, prior experience with all assays is not expected. These assays include: - HPLC chromatography (SEC, WCX, HIC) - Sizing: Dynamic light scattering (DLS), Analytical centrifugation (SV-AUC) - Lab Chip - Nephelometry - icIEF - Viscosity measurements - Fluorescent and Circular dichroism (CD) spectroscopies  skills: HPLC, MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $40.00 - 45.77 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Responsible for the execution and analysis of experiments and analytical procedures.Display an investigative or technological orientation in designing, executing and interpreting experiments and analytical procedures.Investigate basic technical problems and performs routine scientific procedures and experiments under general supervision.Plan and prioritize concurrent experimental procedures. Integrate, compile, and tabulate data and assist supervisor in the analysis and interpretation of the results.May provide oral presentations on results to other department members.Work under active supervision.Follow established procedures.Work is reviewed for soundness of technical judgment and overall adequacy and accuracy.Contribute to the completion of milestones associated with specific projects. Failure to achieve results or erroneous execution may cause delays in program schedules, and may result in the allocation of additional resources.Frequent internal company contacts. Infrequent inter- departmental and outside constituent contacts on routine matters.  qualifications: Years of Experience: 6 - 9 YearsThis role requires execution of several assays. However, prior experience with all assays is not expected. These assays include: - HPLC chromatography (SEC, WCX, HIC) - Sizing: Dynamic light scattering (DLS), Analytical centrifugation (SV-AUC) - Lab Chip - Nephelometry - icIEF - Viscosity measurements - Fluorescent and Circular dichroism (CD) spectroscopies  skills: HPLC, MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • framingham, massachusetts
    • contract
    • $27 - $31.10 per hour
    job summary: Company-Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to making a positive impact on the lives of the patients and families we serve. Our portfolio of transformative therapies, which are marketed in countries around the world, represent groundbreaking and life-saving advances in medicine. As a part of this company, we benefit from the reach and resources of one of the world's largest pharmaceutical companies, with a shared commitment to improving the lives of patients. This position is part of Process Science in Global Manufacturing Science & Analytical Technology (MSAT) and is based at the biologics hub in Boston, MA. The global MSAT team is within the Industrial Affairs (IA) unit of company-Genzyme's Specialty Care organization. The Team is responsible for providing laboratory-based technical support to company biologics. The Team recently designed a state-of-the-art laboratory with capabilities to support small-scale models of the commercial cell culture and purification operations, as well as analytical testing. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $27.00 - 31.10 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Process Science team member will: - Execute protein purification studies using AKTA instrumentation - Perform some protein characterization work such as UV spectrophotometry for protein concentration and HPLC (high performance liquid chromatography) for product purity to support in-process sample testing and quality control - Participate in design and execution of experiments using small-scale models, analyze and interpret results, and recommend additional experiments. Utilize this knowledge to expand process understanding and drive improvements in the commercial manufacturing operations including improving process robustness/reliability. - Apply design space knowledge to support effective investigations and root cause analysis - Use scientific principles and professional practices to solve a range of complex problems in creative and practical ways - Author protocols, technical reports, data analysis summaries, and SOPs   qualifications: - Bachelor's degree or higher in Chemical Engineering, Biochemistry, Biology, or relevant field with 0-3 years of experience - Effective communication & presentation skills - Hands-on experience with AKTA instrumentation for protein purification preferred, but not required   skills: HPLC, SOP, Biology 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: Company-Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to making a positive impact on the lives of the patients and families we serve. Our portfolio of transformative therapies, which are marketed in countries around the world, represent groundbreaking and life-saving advances in medicine. As a part of this company, we benefit from the reach and resources of one of the world's largest pharmaceutical companies, with a shared commitment to improving the lives of patients. This position is part of Process Science in Global Manufacturing Science & Analytical Technology (MSAT) and is based at the biologics hub in Boston, MA. The global MSAT team is within the Industrial Affairs (IA) unit of company-Genzyme's Specialty Care organization. The Team is responsible for providing laboratory-based technical support to company biologics. The Team recently designed a state-of-the-art laboratory with capabilities to support small-scale models of the commercial cell culture and purification operations, as well as analytical testing. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $27.00 - 31.10 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Process Science team member will: - Execute protein purification studies using AKTA instrumentation - Perform some protein characterization work such as UV spectrophotometry for protein concentration and HPLC (high performance liquid chromatography) for product purity to support in-process sample testing and quality control - Participate in design and execution of experiments using small-scale models, analyze and interpret results, and recommend additional experiments. Utilize this knowledge to expand process understanding and drive improvements in the commercial manufacturing operations including improving process robustness/reliability. - Apply design space knowledge to support effective investigations and root cause analysis - Use scientific principles and professional practices to solve a range of complex problems in creative and practical ways - Author protocols, technical reports, data analysis summaries, and SOPs   qualifications: - Bachelor's degree or higher in Chemical Engineering, Biochemistry, Biology, or relevant field with 0-3 years of experience - Effective communication & presentation skills - Hands-on experience with AKTA instrumentation for protein purification preferred, but not required   skills: HPLC, SOP, Biology 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.
    • milford, massachusetts
    • permanent
    • $95,000 - $110,000 per year
    job summary: Job Summary 100% onsite 2nd shift, 3:00pm - 11:30 pm This position is responsible for overseeing daily activities on the designated shift for Downstream operations (purification, formulation, etc) at the Milford MA biomanufacturing facility. In addition to overseeing the daily activities of the associates on the shift, the hands-on Manager will work alongside the associates executing manufacturing operations and batch records assuring that the entire team is in strict compliance with current Good Manufacturing Practices (cGMP), environmental health and safety guidelines and any other regulations that may apply.   location: Milford, Massachusetts job type: Permanent salary: $95,000 - 110,000 per year work hours: 3 to 11 education: Associate   responsibilities: Key Experience/ Responsibilities for Shift Supervisor - Downstream Hands-on supervision of manufacturing staff including hiring, coaching, training, goal-setting, professional development, overall performance management and assessment.Maintain personal training requirements and assure that each team member is adequately trained and documented for the execution of production SOP's and MPR's.Subject Matter Expert in cGMP downstream manufacturing; especially with Chromatography, Column Packing, Tangential Flow Filtration (TFF), Ultrafiltration/Diafiltration (UF/DF), Nanofiltration, Formulation, Bulk Drug Substance Aliquotting.A thorough understanding of purification key performance indicators, column volumes, retention time, resin loading, linear velocity, TFF membrane loading, diafiltration factor, LMM and the science behind the downstream production of mAb's.Specific equipment/systems including Cytiva Single Use Mixers (100L, 200L, 500L, 1000L), Cytiva AKTA Ready chromatography skid, Cytiva AKTA ReadyFlux XL TFF, TCU's, BSC's, Millipore and Sartocheck integrity testers, and disposable technology systems. Must have a thorough understanding of the equipment and controls as this role will be the front-line troubleshooting and correction role for the shift.Author, revise and approve SOP's, batch records, deviations and other documentation as required to ensure compliance.Thoroughly familiar with the identification of actions and results that are outside procedures and limits which require escalation through events and deviations. Responsibilities include leading and completing investigations of root causes and formally documenting/writing deviations for such events in downstream.Subject matter expert for materials and the ordering of materials in time to meet the schedule. Participates in inventory cycle counts and resolution/ corrective actions for discrepancies.Assures that SAP transactions for process orders are executed on time and works with supply chain to resolve any discrepancies.Schedules daily activities for the shift, tracks completion of activities and reports on progress to downstream manufacturing manager.Assures that executed batch records are reviewed thoroughly and all entries are correct before turning over to QA for approval. Works to resolve batch record entry issues before they are reviewed by QA.Leads or oversees new employees' training (as executed on the floor) to understand what new employees are trained to perform and can document in batch record, prevents task execution before training is documented.Assures activities in the suite are conducted safely and in accordance with Safety procedures.   qualifications: Qualifications With high school diploma: Required 5+ years of related experience required or an associate degree in Life Sciences/Engineering field, Biotech Certificate preferred.Also 2+ years experience as a Lead operator, supervisor or manager in Life Sciences. With Bachelor's degree: Required 2-6 years of related experience Demonstrated proficiency in leading a team for 1+ years. Able to read and follow detailed written instructions and have good verbal/written communication skills.Able to write legibly and grammatically correct entries on records. Must be able to author technical procedures and create forms.Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.)Good computer skills, knowledge of Microsoft Word, Excel.Good interpersonal skills and be able to work effectively and efficiently in a team environment.Ability to meet schedule required; this position may include shift, weekend, holiday work and overtime at times, as dictated by the 365-day per year production schedule.Ability to work in a clean room environment and comply with hygiene standards and use of special garments. Additionally, personal protective equipment must be worn due to safety requirements.Proficient in BSC operations and aseptic technique.  skills: Protein Purification, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Job Summary 100% onsite 2nd shift, 3:00pm - 11:30 pm This position is responsible for overseeing daily activities on the designated shift for Downstream operations (purification, formulation, etc) at the Milford MA biomanufacturing facility. In addition to overseeing the daily activities of the associates on the shift, the hands-on Manager will work alongside the associates executing manufacturing operations and batch records assuring that the entire team is in strict compliance with current Good Manufacturing Practices (cGMP), environmental health and safety guidelines and any other regulations that may apply.   location: Milford, Massachusetts job type: Permanent salary: $95,000 - 110,000 per year work hours: 3 to 11 education: Associate   responsibilities: Key Experience/ Responsibilities for Shift Supervisor - Downstream Hands-on supervision of manufacturing staff including hiring, coaching, training, goal-setting, professional development, overall performance management and assessment.Maintain personal training requirements and assure that each team member is adequately trained and documented for the execution of production SOP's and MPR's.Subject Matter Expert in cGMP downstream manufacturing; especially with Chromatography, Column Packing, Tangential Flow Filtration (TFF), Ultrafiltration/Diafiltration (UF/DF), Nanofiltration, Formulation, Bulk Drug Substance Aliquotting.A thorough understanding of purification key performance indicators, column volumes, retention time, resin loading, linear velocity, TFF membrane loading, diafiltration factor, LMM and the science behind the downstream production of mAb's.Specific equipment/systems including Cytiva Single Use Mixers (100L, 200L, 500L, 1000L), Cytiva AKTA Ready chromatography skid, Cytiva AKTA ReadyFlux XL TFF, TCU's, BSC's, Millipore and Sartocheck integrity testers, and disposable technology systems. Must have a thorough understanding of the equipment and controls as this role will be the front-line troubleshooting and correction role for the shift.Author, revise and approve SOP's, batch records, deviations and other documentation as required to ensure compliance.Thoroughly familiar with the identification of actions and results that are outside procedures and limits which require escalation through events and deviations. Responsibilities include leading and completing investigations of root causes and formally documenting/writing deviations for such events in downstream.Subject matter expert for materials and the ordering of materials in time to meet the schedule. Participates in inventory cycle counts and resolution/ corrective actions for discrepancies.Assures that SAP transactions for process orders are executed on time and works with supply chain to resolve any discrepancies.Schedules daily activities for the shift, tracks completion of activities and reports on progress to downstream manufacturing manager.Assures that executed batch records are reviewed thoroughly and all entries are correct before turning over to QA for approval. Works to resolve batch record entry issues before they are reviewed by QA.Leads or oversees new employees' training (as executed on the floor) to understand what new employees are trained to perform and can document in batch record, prevents task execution before training is documented.Assures activities in the suite are conducted safely and in accordance with Safety procedures.   qualifications: Qualifications With high school diploma: Required 5+ years of related experience required or an associate degree in Life Sciences/Engineering field, Biotech Certificate preferred.Also 2+ years experience as a Lead operator, supervisor or manager in Life Sciences. With Bachelor's degree: Required 2-6 years of related experience Demonstrated proficiency in leading a team for 1+ years. Able to read and follow detailed written instructions and have good verbal/written communication skills.Able to write legibly and grammatically correct entries on records. Must be able to author technical procedures and create forms.Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.)Good computer skills, knowledge of Microsoft Word, Excel.Good interpersonal skills and be able to work effectively and efficiently in a team environment.Ability to meet schedule required; this position may include shift, weekend, holiday work and overtime at times, as dictated by the 365-day per year production schedule.Ability to work in a clean room environment and comply with hygiene standards and use of special garments. Additionally, personal protective equipment must be worn due to safety requirements.Proficient in BSC operations and aseptic technique.  skills: Protein Purification, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • milford, massachusetts
    • permanent
    • $60,000 - $85,000 per year
    job summary: Excellent opportunity with a rapidly growing CDMO. We have 3 positions for Upstream Manufacturing Associates. Ideal candidates will have at least one (1) year of cell culture experience in a GMP environment. Offering competitive salaries, benefits, annual bonuses and a $2,500 sign on bonus. Current Openings: Sunday to Wednesday, 7AM to 5:30PM (2)Monday to Friday, 7AM to 3:30 PM (1)   location: Milford, Massachusetts job type: Permanent salary: $60,000 - 85,000 per year work hours: 7 to 3 education: High School   responsibilities: Duties and Responsibilities Perform operations of the following (may be applicable to commercial scale product, development studies, clinical scale or validation activities). Operate manufacturing process equipment to perform various manufacturing production steps Knowledge on initiating new revisions for proceduresProficient operating inside of a BSC, sampling, and performing with aseptic techniques.Monitor and record batch parameters, including computer data entry. Complete relevant paperwork following GMP/GDP guidelines.Troubleshoot process problems and respond to alarms. Provide information for unplanned events, including entering data into event management softare.Order, receive and distribute supplies into production area as needed.Demonstrate procedures as a part of training sessions for other team members; may schedule department or process activities which could involve coworkers. Participate in (and may lead, as requested) team meetings and facilitate multidepartment discussions. Convey information to external stake holders (auditors, global colleagues, etc.). Provide support for groups that support manufacturing.Participate on Continuous Improvement Teams.May perform other duties as assigned. (During Production Processing these activities may increase) Manufacturing operations tasks requires operator to regularly remain on feet for shift.Pushing buffer containers ranging from 50L to 200L.Sitting for periods of 2 to 3 hours.Demonstrated knowledge of CGMP manufacturing.Knowledge of laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, chromatography skids and columns, analytical equipment.Proficiency in a variety of mathematical disciplines and able to work with both the metric and USA standards of measurement, and military time.Able to read and follow detailed written instructions and have good verbal/written communication skills.Able to write legibly and grammatically correct entries on records. Must be able to author technical procedures and create forms.Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.)Good computer skills, knowledge of Microsoft Word, Excel.Good interpersonal skills and be able to work effectively and efficiently in a team environment.Ability to meet schedule required; this position may include shift, weekend holiday work and overtime at times, as dictated by the 365-day per year production schedule. Ability to work in a clean room environment and comply with hygiene standards and use of special garments. Additionally, personal protective equipment must be worn due to safety requirements. Such additional responsibilities as the Company may also assign.   qualifications: Qualifications Level I With high school diploma: Normally requires 0-3 years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred.With Bachelor's degree: Normally requires 0-2 years of related experience.Good with Microsoft Office - Outlook, Word, Excel. Level II With high school diploma: Normally requires 1-4 years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred.With Bachelor's degree: Normally requires 0-2 years of related experience.Good with Microsoft Office - Outlook, Word, Excel. Level III With high school diploma: Normally requires 3-6 years of related experience required or an Associate's Degree in Life Sciences/Engineering field. Biotech Certificate preferredWith Bachelor's degree: Normally requires 1-4 years of related experienceDemonstrated knowledge of CGMP manufacturing.Knowledge of laboratory and pharmaceutical production equipmentCell culture experience  skills: Analytical Chemistry, Biology, Cell Cultures, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Excellent opportunity with a rapidly growing CDMO. We have 3 positions for Upstream Manufacturing Associates. Ideal candidates will have at least one (1) year of cell culture experience in a GMP environment. Offering competitive salaries, benefits, annual bonuses and a $2,500 sign on bonus. Current Openings: Sunday to Wednesday, 7AM to 5:30PM (2)Monday to Friday, 7AM to 3:30 PM (1)   location: Milford, Massachusetts job type: Permanent salary: $60,000 - 85,000 per year work hours: 7 to 3 education: High School   responsibilities: Duties and Responsibilities Perform operations of the following (may be applicable to commercial scale product, development studies, clinical scale or validation activities). Operate manufacturing process equipment to perform various manufacturing production steps Knowledge on initiating new revisions for proceduresProficient operating inside of a BSC, sampling, and performing with aseptic techniques.Monitor and record batch parameters, including computer data entry. Complete relevant paperwork following GMP/GDP guidelines.Troubleshoot process problems and respond to alarms. Provide information for unplanned events, including entering data into event management softare.Order, receive and distribute supplies into production area as needed.Demonstrate procedures as a part of training sessions for other team members; may schedule department or process activities which could involve coworkers. Participate in (and may lead, as requested) team meetings and facilitate multidepartment discussions. Convey information to external stake holders (auditors, global colleagues, etc.). Provide support for groups that support manufacturing.Participate on Continuous Improvement Teams.May perform other duties as assigned. (During Production Processing these activities may increase) Manufacturing operations tasks requires operator to regularly remain on feet for shift.Pushing buffer containers ranging from 50L to 200L.Sitting for periods of 2 to 3 hours.Demonstrated knowledge of CGMP manufacturing.Knowledge of laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, chromatography skids and columns, analytical equipment.Proficiency in a variety of mathematical disciplines and able to work with both the metric and USA standards of measurement, and military time.Able to read and follow detailed written instructions and have good verbal/written communication skills.Able to write legibly and grammatically correct entries on records. Must be able to author technical procedures and create forms.Familiar with standard troubleshooting approaches (problem statement, root cause analysis, corrections, etc.)Good computer skills, knowledge of Microsoft Word, Excel.Good interpersonal skills and be able to work effectively and efficiently in a team environment.Ability to meet schedule required; this position may include shift, weekend holiday work and overtime at times, as dictated by the 365-day per year production schedule. Ability to work in a clean room environment and comply with hygiene standards and use of special garments. Additionally, personal protective equipment must be worn due to safety requirements. Such additional responsibilities as the Company may also assign.   qualifications: Qualifications Level I With high school diploma: Normally requires 0-3 years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred.With Bachelor's degree: Normally requires 0-2 years of related experience.Good with Microsoft Office - Outlook, Word, Excel. Level II With high school diploma: Normally requires 1-4 years of related experience required or an associate degree in Life Sciences/Engineering field. Biotech Certificate preferred.With Bachelor's degree: Normally requires 0-2 years of related experience.Good with Microsoft Office - Outlook, Word, Excel. Level III With high school diploma: Normally requires 3-6 years of related experience required or an Associate's Degree in Life Sciences/Engineering field. Biotech Certificate preferredWith Bachelor's degree: Normally requires 1-4 years of related experienceDemonstrated knowledge of CGMP manufacturing.Knowledge of laboratory and pharmaceutical production equipmentCell culture experience  skills: Analytical Chemistry, Biology, Cell Cultures, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.EOEDisclaime For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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