Hybrid in Farmingdale, New Jersey
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Today
5+ years hands-on experience in pharmaceutical, medical device, or life sciences QA Proven track record with 21 CFR Part 11 compliance validation and Computer Systems Validation (CSV) Deep understanding of FDA regulations, GxP requirements, and data integrity Experience supporting FDA approval processes and regulatory submissions Experience with test management tools (Jira, TestRail, qTest, Xray, Zephyr) Proficiency in validation documentation (IQ/OQ/PQ, VMP, RTM, URS/FDS) Bachelor's degre
Easy Apply
Contract
Depends on Experience


















