GMP Technical Writer: Biologics Batch Records
Listed on 2026-10-18
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Manufacturing / Production
Pharmaceutical Manufacturing -
Quality Assurance - QA/QC
Millipore Sigma is seeking a GMP Technical Writer in St. Louis, MO to create batch records for GMP manufacturing of a new biologic drug substance.
You will work with Manufacturing, Process & Analytical Development, Quality, and Project Management to develop robust Tech Transfer documents, ensuring accuracy and compliance. The role requires strong composition and writing skills, with deep knowledge of GMP equipment and processes, and the ability to communicate effectively with internal teams and
We are looking to fill the GMP Technical Writer:
Biologics Batch Records position at Emd Group in St. Louis, MO, United States.
We would love to welcome a new GMP Technical Writer:
Biologics Batch Records to our team in St. Louis, MO, United States.
For the GMP Technical Writer:
Biologics Batch Records position at Emd Group, we are reviewing applications now.
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