Manufacturing Associate

We 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 Biotech Manufacturing Associate, you...

Job DescriptionJob DescriptionLooking for an exciting career with the opportunity to grow from within?  Affinity recruiting is looking for talented Manufacturing Operator Leads to join an amazing and growing manufacturing company in the Norwood, MA!The right person will have the opportunity to move up within the organization!This position is a cross between...

The RoleIn this role, you will the Engineer I will play a key part in enhancing and leading our cutting-edge manufacturing processes and will serve as either a technical liaison for capital projects or for GMP manufacturing process equipment at Modernas manufacturing facility in Norwood, MA. This role will support the reduction of manufacturing events, will...

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...

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...

Job OverviewAre you seeking an entry-level opportunity with a chance to advance in a dynamic and expanding organization? Affinity Recruiting is currently in search of a Purchasing Associate to support a local manufacturing firm.In this position, you will engage in a range of procurement activities and administrative tasks under the guidance of the Purchasing...

Job OverviewAre you seeking an entry-level opportunity with a chance to advance in a dynamic and expanding organization? Affinity Recruiting is in search of a Purchasing Associate to support a local manufacturing firm.In this position, you will engage in a range of procurement activities and administrative tasks under the guidance of the Purchasing Material...

Job DescriptionJob DescriptionLooking for an entry level position and a chance to grow with an amazing and growing company?  Affinity recruiting is looking for a Purchasing Associate for a local manufacture in the Norwood, MA location.In this role you will perform a variety of purchasing tasks and other clerical functions under the direction of the...

There are 4 shifts available below in the body of this message.The fastest way to get considered is to email me your resume to my work email and your top 2 shift choices to my email: michael.anderson@randstadusa.comAlso still apply here on the LI postin I have as a back-up...Randstad Life Sciences has several contract openings onsite with a pharmaceutical in...

There are 4 shifts available below in the body of this message. The fastest way to get considered is to email me your resume to my work email and your top 2 shift choices to my email: michael.anderson@randstadusa.com Also still apply here on the LI postin I have as a back-up... Randstad Life Sciences has several contract openings onsite with a...

There are 4 shifts available below in the body of this message.The fastest way to get considered is to email me your resume to my work email and your top 2 shift choices to my email: michael.anderson@randstadusa.comAlso still apply here on the LI postin I have as a back-up...Randstad Life Sciences has several contract openings onsite with a pharmaceutical in...

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 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 RoleReporting to the Sr. Director of Sterility Assurance, the Associate Director of Sterility Assurance is tasked with leading the development and management of an aseptic and sterility assurance program for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role encompasses overseeing operational readiness for clinical and...

The RoleReporting to the Sr. Director of Sterility Assurance, the Associate Director of Sterility Assurance is tasked with leading the development and management of an aseptic and sterility assurance program for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role encompasses overseeing operational readiness for clinical and...

The RoleReporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational readiness for production of both clinical and commercial drug products while adhering...

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...

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 Description6 Month ContractNorwood, MAPR: $25-34/hourShift: M-F, 2nd Shift Job SummaryReporting to the Supervisor of Quality Control, Seeking a Quality Control Raw Materials Associate I, Sampler based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further...

The Role:The Associate Director, Global Regulatory Science CMC Therapeutics Programs, will be responsible for leading regulatory CMC strategy and support for products in clinical development (IND, CTA) and commercial product registrations (BLA, MAA), including, post-approval variations. The Associate Director will be responsible for developing regulatory...