Pace Life Sciences is seeking a Technical Writer for on-site work in Oakdale, MN. You will author, revise, and maintain GMP documentation supporting compliant operations in a regulated lab environment.
Responsibilities include coordinating investigations, CAPAs, change controls, and SOPs, and translating complex data into clear documentation. A Life Sciences/QA/technical communication background is required.
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GMP QA Technical Writer - Documentation Expert
Pacelabs · Oakdale, MN, USA ·
- Job type:
- Full Time