Upstream GMP Documentation Specialist - Biopharma
Listed on 2026-10-18
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Pharmaceutical
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Healthcare
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.
We would love to welcome a new Upstream GMP Documentation Specialist
- Biopharma to our group in Milford, MA, United States.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Upstream GMP Documentation Specialist
- Biopharma role at Rentschler Biopharma, Inc., based in Milford, MA, United States.
We are looking to fill the Upstream GMP Documentation Specialist
- Biopharma position at Rentschler Biopharma, Inc. in Milford, MA, United States.
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