Pharma Validation Specialist: cGMP & QA
Listed on 2026-10-07
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Actalent seeks a Validation Associate / Lab Tech to support equipment validation, environmental monitoring, and cleaning validation in a pharmaceutical manufacturing setting. You will collaborate with chemistry, biology, QA, QC, and manufacturing teams to ensure compliant production processes.
The role emphasizes strong analytical skills, attention to detail, and effective cross-functional communication to drive continuous improvement and adherence to FDA and cGMP standards.
Step into the Pharma Validation Specialist: cGMP & QA role at Actalent in Boca Raton, FL, United States and grow with us.
The position is based in Boca Raton, FL, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 44.000 - 47.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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