Quality Assurance & Documentation Specialist
Listed on 2026-10-15
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Regulatory Compliance Specialist, Quality Control - QC Analysts/Managers, Production QC/QA
Nucleus Biologics, The Cell Performance Company, San Diego, CA, is seeking a Quality Specialist to support QA and document control within a cGMP environment. You will manage controlled documents, release manufacturing and batch records, oversee change requests, and assist audits.
The role requires 2–4 years in QA/document control, familiarity with GMP/ISO/FDA standards, and experience with eQMS (ZenQMS preferred). Strong attention to detail and cross-functional collaboration are essential.
We would love to welcome a new Quality Assurance & Documentation Specialist to our team in San Diego, CA, United States.
This is a great opening to take on the Quality Assurance & Documentation Specialist role at Nucleus Biologics.
As a Quality Assurance & Documentation Specialist, you will play an important part at Nucleus Biologics in San Diego, CA, United States.
We invite applications for the Quality Assurance & Documentation Specialist position located in San Diego, CA, 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).