Manufacturing Associate Position

Job Title: Production AssociateAbout the Job:Industry leading Manufacturing company is seeking a Production Associate to join their team. As a Production Associate, you will be responsible for working on computer systems to read instructions and batch records, as well as moving product throughout the facility.Key Responsibilities:• Working on computer...

Job DescriptionJob DescriptionJoin a Leading Biopharmaceutical Company Through Randstad!Are you ready to start a fulfilling career in biopharmaceutical manufacturing? Randstad, in partnership with one of the world’s leading biopharmaceutical companies, is seeking passionate individuals to join as Manufacturing Associates in Norwood, MA. If you’re eager...

Job DescriptionJob DescriptionRandstad in partnership with one of the largest pharmaceutical companies in the world is seeking a cGMP Associate to support GMP Manufacturing of biopharmaceuticals on-site in Norwood, MA.The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based personalized medicine for evaluation in...

Job DescriptionJob DescriptionRandstad in partnership with one of the largest pharmaceutical companies in the world is seeking a cGMP Associate to support GMP Manufacturing of biopharmaceuticals on-site in Norwood, MA.The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based personalized medicine for evaluation in...

Job DescriptionJob DescriptionWe are pioneers in harnessing the power of mRNA technology to develop groundbreaking therapies and vaccines that have the potential to transform lives. Our state-of-the-art manufacturing facility is dedicated to producing high-quality mRNA-based products that address unmet medical needs globally.As a Manufacturing Associate, you...

Competitive Opportunities in mRNA-Based ProductionAs a leader in harnessing the power of mRNA technology, we are seeking a skilled Manufacturing Associate to contribute to the production of groundbreaking therapies and vaccines. Our state-of-the-art manufacturing facilities, located in Burlington, MA, and Norwood, MA, are dedicated to producing high-quality...

The RoleIn this role, you will execute, proficiently under guidance, all applicable manufacturing unit operations, following relevant standard operating procedures and cGMP regulations. The work is conducted within a clean-room environment and typically involves limited physical activity including lifting and standing for periods of time.Heres What Youll...

Job DescriptionJob DescriptionShape the Future of Medicine with Randstad!Randstad, in partnership with a leading biopharmaceutical company, is seeking motivated individuals to join their team in Norwood, MA, as Manufacturing Operations Specialists. If you’re ready to contribute to groundbreaking mRNA-based medicines and thrive in a dynamic, hands-on...

Job Summary:The Logistics Associate II will play a crucial role in supporting the movement of materials to meet the manufacturing teams' needs in the Norwood facilities, as well as the Clinical site in Burlington, Production in Cambridge, and the Quality Control labs in Dedham. This position will be responsible for creating area-specific stock transport...

Job DescriptionJob DescriptionIMMEDIATELY HIRING Are you ready to join a groundbreaking biotech company leader in mRNA technology? Join us to start shaping the future of pharmaceutical manufacturing as pioneers in harnessing the power of mRNA technology creating innovative medicines and vaccines If you want to be part of a team that's making history...

Job DescriptionJob DescriptionRandstad in partnership with one of the largest pharmaceutical companies in the world is seeking a cGMP Associate for mRNA Manufacturing of pharmaceuticals Night shift. These are 12 hour rotating shifts. (pitman schedule) The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based...

The Document Control Associate is responsible for managing global quality documentation in compliance with ISO standards. The role requires 3-5 years of relevant experience, strong proficiency in Microsoft Office, Oracle, and data visualization tools, along with excellent organizational and communication skills​Client DetailsMy client is a well-established...

Job SummaryWe are seeking an experienced Associate Director to lead our CMC Program Management team in Technical Development. The ideal candidate will have a strong background in science and prior experience in Manufacturing, Quality, Process Development, and/or Supply Chain organizations.The Associate Director will be responsible for leading pivotal work...

Job DescriptionJob DescriptionRandstad is hiring several people to work as Material Handlers/Logistics Associates with our client, a leading pharmaceutical company in Norwood. In this role, you will be part of a cohesive team responsible for producing GMP mRNA-based medicines for evaluation in human clinical trials.You will support the handling and...

The Role: The Associate Director, Global Regulatory Science - CMC will be responsible for leading regulatory CMC strategy and execution for one or more programs. The Associate Director will be responsible for developing global regulatory CMC strategies and collaborating with key stakeholders to execute the strategies in alignment with regulatory requirements...

The Role: The Associate Director, Global Regulatory Science - CMC will be responsible for leading regulatory CMC strategy and execution for a commercial product, including most notably, post-approval variations. The Associate Director will be responsible for developing US regulatory CMC strategies and collaborating with key stakeholders to execute the...

Job DescriptionJob DescriptionWe are looking for a dedicated Quality Control Laboratory Associate to join our team. In this role, you will perform routine Good Manufacturing Practice (GMP) testing and support various laboratory activities at Moderna’s manufacturing facility and affiliated contract organizations. Your focus will be on molecular and cell...

Job DescriptionJob DescriptionJob Title: Associate I, Quality Control ChemistryLocation: Norwood MAPay: $30-36/hrShift: Wed-Sat 8am-6pm The RoleIn this role, you will perform cGMP QC Chemistry testing for QC Chemistry, release, stability and in process samples. This role may support special projects as needed. This role will be working 1st shift (8am-...

Job Details The Role: The Associate Director, Global Regulatory Science - CMC will be responsible for leading regulatory CMC strategy and execution for a commercial product, including most notably, post-approval variations. The Associate Director will be responsible for developing US regulatory CMC strategies and collaborating with key stakeholders to...

Job SummaryWe are seeking an experienced Associate Director to lead our GxP Systems Application Management Services team. The successful candidate will be responsible for overseeing the management of our digital quality GxP systems, ensuring compliance with regulatory requirements and driving continuous improvement.The ideal candidate will have a strong...

Job DescriptionJob DescriptionEmbrace a thrilling opportunity to work with a leading biotechnology company that is revolutionizing healthcare through groundbreaking mRNA technology. Join a dynamic team of scientists and researchers dedicated to developing life-changing vaccines and therapeutics. At this innovative organization, you'll have the chance to...