QA Documentation Lead — MasterControl & cGMP Compliance
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager -
Pharmaceutical
Regulatory Compliance Specialist
Tris Pharma, Inc. in Monmouth, NJ seeks a Quality Assurance Documentation Lead to support QA with documentation control and compliance with SOPs, cGMPs, and FDA standards.
The role involves Master Control, DCR PKTs, specs, test methods, stability protocols, MBRs, and change control to ensure properly implemented changes and robust documentation across departments in a fast-paced biotech setting.
We are looking to fill the QA Documentation Lead — Master Control & cGMP Compliance position at Tris Pharma, Inc. in NJ, United States.
Join us at Tris Pharma, Inc. as our next QA Documentation Lead — Master Control & cGMP Compliance in NJ, United States.
We are currently recruiting a QA Documentation Lead — Master Control & cGMP Compliance for our team in NJ, United States.
This is a great opportunity to take on the QA Documentation Lead — Master Control & cGMP Compliance role at Tris Pharma, Inc.
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