QA Documentation Lead — MasterControl & cGMP Compliance
Listed on 2026-09-18
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
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.
Join us at Tris Pharma, Inc. as our next QA Documentation Lead — Master Control & cGMP Compliance in NJ, United States.
Our group is growing, and we are hiring a QA Documentation Lead — Master Control & cGMP Compliance in NJ, United States.
This opening is for the QA Documentation Lead — Master Control & cGMP Compliance role at Tris Pharma, Inc.
We are seeking a motivated QA Documentation Lead — Master Control & cGMP Compliance to join Tris Pharma, Inc. in NJ, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).