Upstream GMP Documentation Specialist - Biopharma
Listed on 2026-10-07
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Pharmaceutical
Rentschler Biopharma, Inc. in Milford, MA is seeking a Manufacturing Technical Writer on a 6+ month contract.
The role focuses on creating, revising GMP documentation including MPRs, batch records, SOPs and work instructions for upstream processes. You will own document workflows, ensure accuracy and on-time delivery, and collaborate with Operations, MSAT, Process Engineering, QA and Training to align training with documentation changes.
As a Upstream GMP Documentation Specialist - Biopharma, you will play an important part at Rentschler Biopharma, Inc. in Milford, MA, United States.
The position is based in Milford, MA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is - .
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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