GMP Technical Writer – QMS & Investigations; Onsite
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Quality Assurance - QA/QC
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Healthcare
Medical Science
Job Description & How to Apply Below
Pace Life Sciences in Oakdale, MN is hiring a Technical Writer onsite. You will author, update, and manage GMP documentation within a regulated contract testing environment, coordinating with Operations, Laboratory, and Quality Assurance to ensure inspection readiness and compliance with cGMP and data integrity standards.
This full-time role offers strong growth and a comprehensive benefits package. Qualified candidates have a Bachelor’s in Life Sciences and 3+ years in GMP settings, with
As a GMP Technical Writer – QMS & Investigations (Onsite), you will play an important part at Pace Analytical Life Sciences in Oakdale, MN, United States.
This posting is for the GMP Technical Writer – QMS & Investigations (Onsite) role at Pace Analytical Life Sciences, based in Oakdale, MN, United States.
We are looking to fill the GMP Technical Writer – QMS & Investigations (Onsite) position at Pace Analytical Life Sciences in Oakdale, MN, United States.
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