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
job summary: Shift: Monday - Friday 4:00pm -2:30am (Friday shift would be 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 manuf
job summary: Shift: Monday - Friday 4:00pm -2:30am (Friday shift would be 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 manuf
We are seeking a Distribution Specialist to oversee and coordinate distribution processes with third-party logistics (3PL) partners. This role ensures efficient order processing, accurate inventory management, and timely product delivery. The ideal candidate will work closely with warehouse teams, logistics providers, and internal departments to optimize operations and maintain compliance with industry standards.salary: $30 - $35 per hourshift: F
We are seeking a Distribution Specialist to oversee and coordinate distribution processes with third-party logistics (3PL) partners. This role ensures efficient order processing, accurate inventory management, and timely product delivery. The ideal candidate will work closely with warehouse teams, logistics providers, and internal departments to optimize operations and maintain compliance with industry standards.salary: $30 - $35 per hourshift: F
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 - &#
The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements. The Supervisor leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s)
The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements. The Supervisor leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s)
job summary: Client is targeting a Lab Manager with previous experience overseeing and running a lab. Synthetic lab experience will be a plus. location: Cambridge, Massachusetts job type: Contract salary: $45 - 51 per hour work hours: 9 to 5 education: High School responsibilities: Management of the DSTS laboratories: Drive organization and improve productivity of facility through adherence to 5S principles.Create and maintain digital
job summary: Client is targeting a Lab Manager with previous experience overseeing and running a lab. Synthetic lab experience will be a plus. location: Cambridge, Massachusetts job type: Contract salary: $45 - 51 per hour work hours: 9 to 5 education: High School responsibilities: Management of the DSTS laboratories: Drive organization and improve productivity of facility through adherence to 5S principles.Create and maintain digital
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
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: Shift: Sun-Wed 10am - 8pm In this role, you will perform routine environmental monitoring and critical utility (WFI and Gas) Sampling at the company's manufacturing facilities in support of both Clinical and Commercial Manufacturing Operations. location: Norwood, Massachusetts job type: Contract salary: $30 - 38 per hour work hours: 11 to 7 education: Bachelors responsibilities: Conduct Environmental Monitoring (Rout
job summary: Shift: Sun-Wed 10am - 8pm In this role, you will perform routine environmental monitoring and critical utility (WFI and Gas) Sampling at the company's manufacturing facilities in support of both Clinical and Commercial Manufacturing Operations. location: Norwood, Massachusetts job type: Contract salary: $30 - 38 per hour work hours: 11 to 7 education: Bachelors responsibilities: Conduct Environmental Monitoring (Rout
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
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
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: 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: 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 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: 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
