Pace® Life Sciences seeks a Technical Writer to author, coordinate, and maintain GMP documentation in a regulated contract testing laboratory environment in Oakdale, MN. You will produce SOPs, work instructions, CAPAs, investigations, deviations, and change controls, ensuring accuracy and inspection readiness.
Collaborating with Operations, Laboratory, and QA, you will translate complex lab and process data into clear documentation, support audits, and drive continuous improvement within a
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Onsite GMP Technical Writer – Quality & Compliance
Pace® Analytical Services · Oakdale, MN, USA ·
- Job type:
- Contract