CGMP Cell & Gene Therapy Manufacturing Lead
Listed on 2026-11-07
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Research/Development
Regulatory Compliance Specialist
UC Irvine is seeking a scientifically skilled professional to bridge bench research with clinical-scale GMP manufacturing of cell therapies. You will lead process development, supervise sterile production, and ensure strict GMP/GLP compliance across ISO clean rooms.
The role demands strong collaboration, rigorous documentation, and hands-on leadership to drive autologous and allogeneic therapy workflows from development to clinical readiness at our Irvine facilities.
We would love to welcome a new cGMP Cell & Gene Therapy Manufacturing Lead to our team in Irvine, CA, United States.
The position is based in Irvine, CA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health.
The advertised compensation is 90..
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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