Quality Assurance Documentation Lead: MasterControl & Stability Expert
Listed on 2026-10-11
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Tris Pharma, Inc. in Monmouth, NJ is seeking a Quality Assurance Documentation Lead to support the QA function and ensure manufacturing quality controls comply with SOPs, cGMPs and FDA standards.
Under QA Mgmt, you will handle day-to-day operational QA activities across multiple departments, maintain GxP records, support Master Control systems, and ensure timely APR sub-reports for resin-based ER tablets and related products. Fluency in English is required. Background checks may be conducted.
Step into the Quality Assurance Documentation Lead:
Master Control & Stability Expert role at Tris Pharma, Inc in South Brunswick, NJ, United States and grow with us.
The Quality Assurance Documentation Lead:
Master Control & Stability Expert position in the Bio & Pharmacology & Health, Management & Operations field is open for applications.
We have an opening for a Quality Assurance Documentation Lead:
Master Control & Stability Expert in South Brunswick, NJ, United States within Bio & Pharmacology & Health, Management & Operations.
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