About this opportunity
Tris Pharma, Inc lists this Quality Assurance Documentation Lead: MasterControl & Stability Expert opportunity in south brunswick, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.