Radiopharmaceutical Production Chemist II: GMP & Process Lead
Listed on 2026-10-17
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Pharmaceutical
Pharmaceutical Manufacturing, Validation Engineer, Pharma Engineer -
Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer
SOFIE in Totowa, NJ, seeks a Pharmaceutical Production Chemist II to support the production of radiopharmaceuticals under GMP and 21 CFR 211. You will operate automated equipment, lead process transfers, and ensure regulatory compliance.
The role requires collaboration with partners and adherence to hazardous materials safety guidelines. Responsibilities include equipment maintenance, batch processing in clean rooms (ISO-7/ISO-5), deviation reporting, SOP and validation work, and packaging
Our group is growing, and we are hiring a Radiopharmaceutical Production Chemist II: GMP & Process Lead in Totowa, NJ, United States.
The position is based in Totowa, NJ, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 85.000 - 90.000.
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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