QA Documentation Lead: MasterControl & GMP Compliance
Listed on 2026-10-01
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Tris Pharma, Inc. seeks a Quality Assurance Documentation Lead to support QA compliance with SOPs, cGMPs, and FDA standards at our Monmouth, NJ site.
Under QA management, you will maintain Master Control docs, support stability programs and APR data, and collaborate with multiple departments to ensure timely, accurate records and change controls.
Fluency in English is required; background checks may be conducted. Wage: $77,522–$101,750 plus comprehensive benefits.
We are looking to fill the QA Documentation Lead:
Master Control & GMP Compliance position at Merck & Co. in South Brunswick, NJ, United States.
Learn more about the QA Documentation Lead:
Master Control & GMP Compliance role in the description above.
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