job summary: A large, multinational medical device company is seeking Medical Device Toxicologists to review product documentation and determine compliance status per ISO 10993 series of standards. location: Telecommute job type: Contract salary: $30.00 - 33.33 per hour work hours: 9 to 5 education: No Degree Required responsibilities: Solely focused on reviewing documentation and confirming evidence.Prior experience conducting biocompa
job summary: A large, multinational medical device company is seeking Medical Device Toxicologists to review product documentation and determine compliance status per ISO 10993 series of standards. location: Telecommute job type: Contract salary: $30.00 - 33.33 per hour work hours: 9 to 5 education: No Degree Required responsibilities: Solely focused on reviewing documentation and confirming evidence.Prior experience conducting biocompa
job summary: A large, multinational medical device company is seeking Medical Device Toxicologists to review product documentation and determine compliance status per ISO 10993 series of standards. location: Telecommute job type: Contract salary: $30.00 - 33.33 per hour work hours: 9 to 5 education: No Degree Required responsibilities: Solely focused on reviewing documentation and confirming evidence.Conducting biocompatibility assessme
job summary: A large, multinational medical device company is seeking Medical Device Toxicologists to review product documentation and determine compliance status per ISO 10993 series of standards. location: Telecommute job type: Contract salary: $30.00 - 33.33 per hour work hours: 9 to 5 education: No Degree Required responsibilities: Solely focused on reviewing documentation and confirming evidence.Conducting biocompatibility assessme
Are you looking for an opportunity to contribute to groundbreaking advancements in biotechnology? We are committed to transforming medicine and improving lives. As an Associate, Document Control and Records Management, you will play a crucial role in ensuring compliance and accuracy in our document management processes. If you are detail-oriented, thrive in a regulated environment, and are eager to be part of a high-impact team, we encourage you to apply!s
Are you looking for an opportunity to contribute to groundbreaking advancements in biotechnology? We are committed to transforming medicine and improving lives. As an Associate, Document Control and Records Management, you will play a crucial role in ensuring compliance and accuracy in our document management processes. If you are detail-oriented, thrive in a regulated environment, and are eager to be part of a high-impact team, we encourage you to apply!s
job summary: The Associate, Quality Assurance Documentation, will assist in maintaining and administering all aspects of the GMP document control system compliant with international cGMP expectations and Company policies and procedures. location: Marlborough, Massachusetts job type: Contract salary: $24 - 29 per hour work hours: 9 to 5 education: Bachelors responsibilities: Document Issuance Support: Assist with the issuance of GxP doc
job summary: The Associate, Quality Assurance Documentation, will assist in maintaining and administering all aspects of the GMP document control system compliant with international cGMP expectations and Company policies and procedures. location: Marlborough, Massachusetts job type: Contract salary: $24 - 29 per hour work hours: 9 to 5 education: Bachelors responsibilities: Document Issuance Support: Assist with the issuance of GxP doc
job summary: Immediate opportunity for a QC Microbiology Associate I to join a leading biotechnology and pharmaceutical company specializing in RNA therapeutics, located in Marlborough, MA. In this role, you will play a key part in the commissioning and qualification of the company's new Marlborough facility. Responsibilities include performing routine environmental monitoring, critical utility sampling (WFI and gas), and gowning. Shedule/Shift: 1st shif
job summary: Immediate opportunity for a QC Microbiology Associate I to join a leading biotechnology and pharmaceutical company specializing in RNA therapeutics, located in Marlborough, MA. In this role, you will play a key part in the commissioning and qualification of the company's new Marlborough facility. Responsibilities include performing routine environmental monitoring, critical utility sampling (WFI and gas), and gowning. Shedule/Shift: 1st shif
job summary: 3rd shift, 10pm - 8am, Wednesday - Saturday The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay, and various Development labs. location: Norwood, Massachusetts job type: Contract salary: $25 - 42 per hour work hours: 3 to 11 education: Bachelors responsibilities: Sample coordination including cross functional collaboration with internal and external lab
job summary: 3rd shift, 10pm - 8am, Wednesday - Saturday The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay, and various Development labs. location: Norwood, Massachusetts job type: Contract salary: $25 - 42 per hour work hours: 3 to 11 education: Bachelors responsibilities: Sample coordination including cross functional collaboration with internal and external lab
Exciting Career Opportunity: Biomanufacturing Associate II – Downstream/Purification Randstad has partnered with a leading RTP Biotech Company to create career opportunities for driven individuals ready to make an impact. This is a temp-to-perm contract role with incredible potential to transform a 6–18-month contract into a full-time career in the biotech industry!. What You’ll Do: As a Biomanufacturing Associate II in Downstream/Purific
Exciting Career Opportunity: Biomanufacturing Associate II – Downstream/Purification Randstad has partnered with a leading RTP Biotech Company to create career opportunities for driven individuals ready to make an impact. This is a temp-to-perm contract role with incredible potential to transform a 6–18-month contract into a full-time career in the biotech industry!. What You’ll Do: As a Biomanufacturing Associate II in Downstream/Purific
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus
job summary: We are seeking a motivated Associate Biochemist - HPLC to support laboratory operations in a fast-paced environment. Responsibilities include conducting experiments, analyzing drug product samples, processing data per SOPs, and ensuring compliance through accurate documentation. Additional duties include contributing to reports, presentations, and regulatory documents, as well as participating in safety, recruiting, and committee efforts. Th
job summary: We are seeking a motivated Associate Biochemist - HPLC to support laboratory operations in a fast-paced environment. Responsibilities include conducting experiments, analyzing drug product samples, processing data per SOPs, and ensuring compliance through accurate documentation. Additional duties include contributing to reports, presentations, and regulatory documents, as well as participating in safety, recruiting, and committee efforts. Th
job summary: Produce pharmaceutical components and products by following current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) within a cleanroom environment. Responsibilities include, but not limited to operation and performance on equipment used in the manufacturing unit processes. Perform the weighing of manufacturing ingredients and the manufacturing of the intermediate formulations. Tasks include documentation, data entry
job summary: Produce pharmaceutical components and products by following current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) within a cleanroom environment. Responsibilities include, but not limited to operation and performance on equipment used in the manufacturing unit processes. Perform the weighing of manufacturing ingredients and the manufacturing of the intermediate formulations. Tasks include documentation, data entry
job summary: Location: Norwood, MA (100% On-Site) Duration: 6 Months (Likely to go much longer) Shift: 1st shift, Mon.-Fri. We are seeking an Associate I, Quality Control Microbiology to support environmental monitoring (EM) and critical utility sampling at our Norwood, MA manufacturing facility. This role will contribute to both clinical and commercial manufacturing operations by ensuring compliance with industry regulations and best practices. locat
job summary: Location: Norwood, MA (100% On-Site) Duration: 6 Months (Likely to go much longer) Shift: 1st shift, Mon.-Fri. We are seeking an Associate I, Quality Control Microbiology to support environmental monitoring (EM) and critical utility sampling at our Norwood, MA manufacturing facility. This role will contribute to both clinical and commercial manufacturing operations by ensuring compliance with industry regulations and best practices. locat
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowled
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowled
job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-quality, compliant labeling documents
job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-quality, compliant labeling documents
job summary: The Drug Metabolism and Disposition group in QTAS has an open position for a Senior /Research Associate Scientist to perform drug metabolism/metabolite identification studies supporting a series of small molecule drug discovery projects. The selected candidate will be responsible for designing and conducting in vitro metID studies, processing the data, and interpreting MS/MS results. It is a fully drug metabolism laboratory-based role. It wou
job summary: The Drug Metabolism and Disposition group in QTAS has an open position for a Senior /Research Associate Scientist to perform drug metabolism/metabolite identification studies supporting a series of small molecule drug discovery projects. The selected candidate will be responsible for designing and conducting in vitro metID studies, processing the data, and interpreting MS/MS results. It is a fully drug metabolism laboratory-based role. It wou
job summary: The Records Management Specialist will play a crucial role in organizing, maintaining, and ensuring the management of GxP documentation to support compliance and operational efficiency. location: Westborough, Massachusetts job type: Contract salary: $29 - 34 per hour work hours: 9 to 5 education: Bachelors responsibilities: Organization & Classification: Develop, implement, and maintain an organized filing system for on-si
job summary: The Records Management Specialist will play a crucial role in organizing, maintaining, and ensuring the management of GxP documentation to support compliance and operational efficiency. location: Westborough, Massachusetts job type: Contract salary: $29 - 34 per hour work hours: 9 to 5 education: Bachelors responsibilities: Organization & Classification: Develop, implement, and maintain an organized filing system for on-si
