US Pharma Lab in North Brunswick, NJ, is seeking a Specialist, Quality Assurance Documentation to write, distribute, collect, store, and maintain our documentation. This role ensures compliance with SOPs, GMP documentation, and 21 CFR Parts 111 and 117, reporting to the QA Manager with a dotted line to Head of QA.

You will coordinate with internal teams to understand processes, author and update SOPs, perform QA on documents, and ensure staff use current versions.