1st Shift, Monday- Thursday, 6:00 AM - 4:30 PMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records and understand
1st Shift, Monday- Thursday, 6:00 AM - 4:30 PMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records and understand
2nd Shift, Monday- Thursday, 4:00 PM - 2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records. Understands a
2nd Shift, Monday- Thursday, 4:00 PM - 2:30 AMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records. Understands a
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: Shift: Monday-Friday, 6am-4:30pm (Friday would be all Overtime pay) Responsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP's and the ability to follow manufactu
job summary: Shift: Monday-Friday, 6am-4:30pm (Friday would be all Overtime pay) Responsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP's and the ability to follow manufactu
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: 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: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment
job summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment
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: 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: 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
Are you passionate about providing top-tier customer support in a dynamic and fast-paced environment? We are seeking a Customer Service Representative to join our team! This role offers an exciting opportunity to work with a leading company in the radiopharmaceutical industry, where your contributions will directly impact healthcare professionals and patients.salary: $24 - $26 per hourshift: Firstwork hours: 10:30 AM - 7 PMeducation: High SchoolR
Are you passionate about providing top-tier customer support in a dynamic and fast-paced environment? We are seeking a Customer Service Representative to join our team! This role offers an exciting opportunity to work with a leading company in the radiopharmaceutical industry, where your contributions will directly impact healthcare professionals and patients.salary: $24 - $26 per hourshift: Firstwork hours: 10:30 AM - 7 PMeducation: High SchoolR
Maintain cleanliness in manufacturing clean rooms, ensuring compliance with cGMP standards. Perform daily cleaning, waste removal, and PPE inventory management. Follow safety protocols, report issues, and assist in maintaining a hygienic production environment. Support clean room readiness for audits and operations.salary: $21.18 - $24.35 per hourshift: Firstwork hours: 6 AM - 2:30 PMeducation: High SchoolResponsibilitiesKey Responsibilities: P
Maintain cleanliness in manufacturing clean rooms, ensuring compliance with cGMP standards. Perform daily cleaning, waste removal, and PPE inventory management. Follow safety protocols, report issues, and assist in maintaining a hygienic production environment. Support clean room readiness for audits and operations.salary: $21.18 - $24.35 per hourshift: Firstwork hours: 6 AM - 2:30 PMeducation: High SchoolResponsibilitiesKey Responsibilities: P
Onsite in Billerica, MA 9:00 AM-6:30 PM, with some weekend work. Provide oversight and technical guidance for daily Outbound Shipment operations ensuring the safe, legal tender of products to our carriers. Responsible to ensure compliance with all relevant distribution laws and regulations. Accountable for the accuracy and traceability for the products in preparation for the shipment process to the transportation carrier network. salary: $25 - &#
Onsite in Billerica, MA 9:00 AM-6:30 PM, with some weekend work. Provide oversight and technical guidance for daily Outbound Shipment operations ensuring the safe, legal tender of products to our carriers. Responsible to ensure compliance with all relevant distribution laws and regulations. Accountable for the accuracy and traceability for the products in preparation for the shipment process to the transportation carrier network. salary: $25 - &#
Onsite in Bedford, MA 3 days per week. Must have Order Management Systems experience. The Business Analyst for the Commercial Order Management Systems (OMS) plays a pivotal role in bridging the gap between business needs and technology solutions. This role involves gathering, analyzing, and documenting business requirements for the OMS, ensuring the system effectively supports the order management process for radio pharmaceutical products. The Business A
Onsite in Bedford, MA 3 days per week. Must have Order Management Systems experience. The Business Analyst for the Commercial Order Management Systems (OMS) plays a pivotal role in bridging the gap between business needs and technology solutions. This role involves gathering, analyzing, and documenting business requirements for the OMS, ensuring the system effectively supports the order management process for radio pharmaceutical products. The Business A
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: Discovery Biotherapeutics and Genetic Medicine is seeking a highly motivated research scientist to join the Cell and Functional Biology group. In this role, you will be responsible for the design and execution of cell- and protein- based functional characterization assays for lead antibody identification/optimization and collaborating to generate stage-gate appropriate in vitro / cellular / in vivo data packages supporting PoC. The ideal cand
job summary: Discovery Biotherapeutics and Genetic Medicine is seeking a highly motivated research scientist to join the Cell and Functional Biology group. In this role, you will be responsible for the design and execution of cell- and protein- based functional characterization assays for lead antibody identification/optimization and collaborating to generate stage-gate appropriate in vitro / cellular / in vivo data packages supporting PoC. The ideal cand
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
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: 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: 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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatm
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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatm
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: 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: 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. 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: 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
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
