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 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
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
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: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
job summary: Job Summary In this role, you will be responsible for providing quality assurance network support for contract manufacturing and testing. You are responsible for ensuring that all batch-related activities, including receipt, review, and release of Bulk Drug Substance (BDS) and Drug Product (DP), are conducted in compliance with regulatory standards. This role is focused on executing Batch Record Release activities following Drug Product CMO R
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: This position is responsible for effectively coordinating documentation and samples received in the Quality Control laboratory in accordance with SOP's. location: Framingham, Massachusetts job type: Contract salary: $25.00 - 28.50 per hour work hours: 8 to 4 education: High School responsibilities: Data entry and filing of laboratory documentationRequest, maintain and return of logbooks used in the Quality Control Sample Ma
job summary: This position is responsible for effectively coordinating documentation and samples received in the Quality Control laboratory in accordance with SOP's. location: Framingham, Massachusetts job type: Contract salary: $25.00 - 28.50 per hour work hours: 8 to 4 education: High School responsibilities: Data entry and filing of laboratory documentationRequest, maintain and return of logbooks used in the Quality Control Sample Ma
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 knowle
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 knowle
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: 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: In this role, you will support in-process and release testing for raw material, drug substance and mRNA drug products produced at Moderna's manufacturing facility and affiliated contract organizations. location: Norwood, Massachusetts job type: Contract salary: $30 - 36 per hour work hours: 3 to 11 education: Bachelors responsibilities: Support testing for raw materials, drug substance and drug product, including generatio
job summary: In this role, you will support in-process and release testing for raw material, drug substance and mRNA drug products produced at Moderna's manufacturing facility and affiliated contract organizations. location: Norwood, Massachusetts job type: Contract salary: $30 - 36 per hour work hours: 3 to 11 education: Bachelors responsibilities: Support testing for raw materials, drug substance and drug product, including generatio
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: 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
job summary: The Analytical Development team is seeking a highly creative and self-motivated candidate to join us for a 6-month contract. This role will support the development of small molecule and oligonucleotide drug substance and drug product by developing innovative analytical technologies and establishing control strategies. This role will be responsible for chromatographic method development guided by analytical quality by design (AQbD) principles
job summary: The Analytical Development team is seeking a highly creative and self-motivated candidate to join us for a 6-month contract. This role will support the development of small molecule and oligonucleotide drug substance and drug product by developing innovative analytical technologies and establishing control strategies. This role will be responsible for chromatographic method development guided by analytical quality by design (AQbD) principles
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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines
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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines
job summary: The Analytical Development team that supports the development of oligonucleotide therapeutics by developing innovative analytical technologies and establishing control strategies is seeking a highly creative and self-motivated candidate. This is a 6-month contract. This role will develop and optimize analytical methods on LCMS systems in the lab in Cambridge, MA campus. This role will also support other relevant oligonucleotide studies using
job summary: The Analytical Development team that supports the development of oligonucleotide therapeutics by developing innovative analytical technologies and establishing control strategies is seeking a highly creative and self-motivated candidate. This is a 6-month contract. This role will develop and optimize analytical methods on LCMS systems in the lab in Cambridge, MA campus. This role will also support other relevant oligonucleotide studies using
job summary: True Title: Clinical Pharmacologist (Director, Clinical Pharmacology) 6-Month Initial Contract Remote | EST hours This role will play a pivotal part in supporting the late-stage clinical development of biologics in the fields of immunology, neurology, and hematology. The ideal candidate will bring deep expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to contribute to regulatory submissions (IND, BLA), clinical study reports (CSR)
job summary: True Title: Clinical Pharmacologist (Director, Clinical Pharmacology) 6-Month Initial Contract Remote | EST hours This role will play a pivotal part in supporting the late-stage clinical development of biologics in the fields of immunology, neurology, and hematology. The ideal candidate will bring deep expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to contribute to regulatory submissions (IND, BLA), clinical study reports (CSR)
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: 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: 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
