Lead Lipid MLV Process Validation Engineer
Listed on 2026-10-17
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Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Regulatory Compliance Specialist
Aerogen Pharma is seeking a Senior Process Validation Engineer to own validation strategy for late-stage and commercial lipid MLV drug products. You will lead process characterization, PPQ, and technology transfer with MSAT and CDMO partners.
The role requires extensive GMP experience, DOE/JMP expertise, and strong cross-functional leadership to drive quality and regulatory readiness across programs.
Our group is growing, and we are hiring a Lead Lipid MLV Process Validation Engineer in Foster City, CA, United States.
The position is based in Foster City, CA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Engineering.
The advertised compensation is 138..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Lead Lipid MLV Process Validation Engineer role in the description above.
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