QA Documentation Lead: MasterControl & GMP Compliance
Listed on 2026-10-11
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
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 would love to welcome a new QA Documentation Lead:
Master Control & GMP Compliance to our group in South Brunswick, NJ, United States.
For the QA Documentation Lead:
Master Control & GMP Compliance position at Tris Pharma, Inc., we are reviewing applications now.
Step into the QA Documentation Lead:
Master Control & GMP Compliance role at Tris Pharma, Inc. in South Brunswick, NJ, United States and grow with us.
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