QA Specialist : CGMP Manufacturing & Compliance
Listed on 2026-11-01
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
SOFIE is seeking a Quality Assurance Specialist I to oversee the QA program and the Quality Management System at the site level, ensuring regulatory compliance for products manufactured under 21 CFR Part 212 and 211 as applicable. You will maintain oversight of quality processes and ensure materials, components, packaging, and finished dosage forms meet specifications.
Collaborating with the Facility Manager and Operations, you will write, review, and implement procedures, conduct site audits,
We are seeking a motivated QA Specialist I: CGMP Manufacturing & Compliance to join SOFIE in NJ, United States.
The position is based in NJ, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 60.000 - 75.000.
We aim to respond to suitable candidates as soon as possible.
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