IT & Software

QA Documentation Lead: MasterControl & GMP Compliance

Merck & Co.

South Brunswick · Nj · United States

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.

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Reference: WJ-5385_3206632

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