Quality Assurance Documentation Lead: MasterControl & Stability Expert

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. #J-18808-Ljbffr Tris Pharma, Inc