Biopharmaceutical Manufacturing Associate

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...

About the RoleWe are seeking an experienced Environmental Health and Safety (EHS) professional to join our team at Moderna. As an EHS Manager, you will play a critical role in supporting the day-to-day EHS operations at our facility in Norwood, MA.Key ResponsibilitiesAssess and manage relevant EHS risks within R&D environments and associated enabling...

About the RoleWe are seeking an experienced Environmental Health and Safety (EHS) professional to join our team at Moderna. As an EHS Manager, you will play a critical role in supporting the day-to-day EHS operations at our facility in Norwood, MA.Key ResponsibilitiesAssess and manage relevant EHS risks within R&D environments and associated enabling...

About the RoleWe are seeking a highly skilled Environmental Health and Safety Manager to join our team at Moderna. As a key member of our EHS team, you will play a critical role in supporting the day-to-day operations of our facility in Norwood, MA.Key ResponsibilitiesAssess and manage relevant EHS risks within R&D environments and associated enabling...

About the RoleWe are seeking a highly skilled and experienced Manufacturing Supervisor to lead our cGMP manufacturing team responsible for producing clinical trial materials. The successful candidate will have a strong background in aseptic filling and labelling, as well as experience in managing a team in a fast-paced manufacturing environment.Key...

Job SummaryWe are seeking a highly skilled and experienced Manufacturing Supervisor to lead our cGMP manufacturing team at our Norwood, MA facility. As a key member of our team, you will be responsible for overseeing the vial filling, visual inspection, labelling, and packaging operations for early phase clinical trial material.Key ResponsibilitiesLead a...

Job OverviewModerna is seeking a highly skilled Senior GxP Automation Engineer to join our team. As a Senior GxP Automation Engineer, you will play a crucial role in the design, development, and implementation of automation solutions for our manufacturing operations. You will work closely with cross-functional teams to ensure the smooth operation of our...

About the RoleWe are seeking a highly skilled Sr. GxP Automation Engineer to join our team at Moderna. As a key member of our manufacturing operations, you will play a critical role in supporting the operation of our cutting-edge Drug Product (Fill Finish) GxP manufacturing systems.Key ResponsibilitiesLead the construction, CSV/CQV, and delivery of...

Job Summary:As a Process Engineer at Randstad, you will play a critical role in ensuring the successful execution of capital projects and the maintenance of GMP manufacturing process equipment. This is a unique opportunity to join a dynamic team and contribute to the development of innovative solutions in the life sciences arena.Responsibilities:Provide...

About the RoleWe are seeking a highly skilled GxP Automation Engineer to join our team at BioSpace, Inc. As a key member of our manufacturing operations, you will play a critical role in supporting the operation of our cutting-edge Drug Product (Fill Finish) GxP manufacturing systems.Key ResponsibilitiesTake an active lead role during the construction,...

Join a leading global manufacturer with lots of opportunity for growth A strong work life balance, primarily remote position About Our Client Our client is a global specialty chemical manufacture that produces materials for high-reliability applications across a variety of diverse market sectors. Continuously growing their business using their...

The RoleIn this role, you will be responsible for supporting the day-to-day EHS operations at the Moderna facility in Norwood, MA. The candidate will play a key role in managing EHS events, conducting investigations, implementing CAPA, owning individual EHS programs, and maintaining compliance with various EHS programs under the guidance of the site EHS...

About the RoleWe are seeking a highly skilled Sr. GxP Automation Engineer to join our team at Moderna. As a key member of our manufacturing operations, you will play a crucial part in supporting the operation of our cutting-edge Drug Product (Fill Finish) GxP manufacturing systems.Key ResponsibilitiesTake an active lead role during the construction, CSV/CQV,...

The RoleModerna is seeking a cGMP Manufacturing Supervisor to lead a cohesive team responsible for manufacturing cGMP mRNA medications for evaluation in human clinical trials. The position is based out of our GMP Manufacturing facility in Norwood, MA. This role is 2nd shift 2PM-12AM Wednesday-Saturday.The individual in this role will be hands-on front-line...

About the RoleModerna's Drug Product Development team is seeking an experienced, innovative, and accomplished leader to join our team. As a Senior Drug Product Development Manager, you will be responsible for leading the development of and execution of drug product strategy, contributing to program leadership, staff development, and growth of the...

The Role:This position is part of Modernas Drug Product Development team responsible for ensuring the translation of mRNA technology into successful dosage form and commercial product from a pharmaceutical sciences and engineering perspective. The incumbent will also provide technical leadership and mentoring to the Drug Product Development (DPD) group,...

Job OverviewThe CMC Program Management team in Technical Development is seeking an Associate Director to lead pivotal work focusing on the design and comprehensive management of CMC program integrated project plans. The ideal candidate will have a background in science with prior experience in Manufacturing, Quality, Process Development, and/or Supply Chain...

Job SummaryThe Associate Director, Global Regulatory Science CMC will lead regulatory CMC strategy and execution for a commercial product, including post-approval variations. This role will develop US regulatory CMC strategies and collaborate with key stakeholders to execute the strategies in alignment with US regulatory requirements and business priorities....

About the Role:The Associate Director, Global Regulatory Science - CMC will be responsible for leading regulatory CMC strategy and execution for a commercial product, including post-approval variations. This role will develop and implement effective regulatory CMC strategies for US submissions, identify regulatory risks, and provide regulatory CMC advice to...

The RoleThe Manufacturing Investigations team is responsible for the day-to-day operational support of clinical and commercial drug substance and clinical drug product processing and release through deviation and CAPA writing. A Sr. Specialist, Manufacturing Investigations, independently exercises discretion and applies expert knowledge of cGMP regulations...