QA Documentation Specialist II – GMP & SOPs
Listed on 2026-10-20
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager -
Pharmaceutical
PCI TRGR Penn Pharmaceutical Services Ltd is seeking a QA Documentation Associate II in San Diego to coordinate the review and approval of GMP documentation across SOPs, batch records, and related materials. You will work with Project Managers and SMEs to revise master batch records for changes and ensure timely project completion.
The role requires 2-4 years in documentation or QA, familiarity with cGMP guidelines, and strong written/verbal communication.
We have an opening for a QA Documentation Specialist II – GMP & SOPs in San Diego, CA, United States within Bio & Pharmacology & Health.
We are currently recruiting a QA Documentation Specialist II – GMP & SOPs for our team in San Diego, CA, United States.
This is an excellent opportunity to take on the QA Documentation Specialist II – GMP & SOPs role at PCI TRGR Penn Pharmaceutical Services Ltd.
(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).