Pace Life Sciences in Oakdale, MN is seeking a full-time onsite Technical Writer to author, coordinate, and maintain GMP documentation and quality records in a regulated contract testing laboratory environment. You will collaborate with Operations, Laboratory, QA, and Program Management to ensure documents are accurate, inspection-ready, and compliant with cGMP and data integrity requirements.
Ideal candidates have a Bachelor's in Life Sciences or related field and 3+ years in regulated
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GMP Technical Writer – QMS & Compliance
Pace Analytical Services, LLC · Oakdale, MN, USA ·
- Job type:
- Contract