Pace Life Sciences is seeking an on-site Technical Writer in Oakdale, MN. You will author, revise, and maintain GMP documentation supporting compliant GMP operations in a regulated testing lab.
Collaboration with Operations, Laboratory, QA, and PM teams to develop and manage SOPs, investigations, CAPAs, and change controls ensures data integrity and inspection readiness. Qualified candidates possess a Life Sciences degree and 3+ years in a regulated environment, with strong documentation, QA,
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GMP Quality Documentation Writer – QMS Specialist
Pace® Analytical Services · Oakdale, MN, USA ·
- Job type:
- Full Time