QA Documentation Lead — Pharma Compliance & MasterControl
Listed on 2026-10-07
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Tris Pharma, Inc. is seeking a Quality Assurance Documentation Lead to support the QA function for cGMP-compliant manufacturing and FDA standards. The role focuses on maintaining quality records, monitoring stability chambers, and ensuring proper change control processes are followed.
You will collaborate with Lab Ops, Product Dev, Eng, Production, QA Ops, and IT to ensure timely, accurate APR sub-reports and strict conformance to SOPs and company policies. Fluency in English is required.
The following role is for a QA Documentation Lead — Pharma Compliance & Master Control with Bio Space.
The position is based in South Brunswick, NJ, United States.
This opportunity is part of our work in Management & Operations, Engineering.
The advertised compensation is 78..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
(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).