Pushing the Frontier by pioneering a new class of fully personalized T cell therapies to treat cancer
June 11
🏢 In-office - Los Angeles
Pushing the Frontier by pioneering a new class of fully personalized T cell therapies to treat cancer
• Led technology transfer for autologous cell therapies into manufacturing • Develop technology transfer strategies for GMP • Author technical documents and reports • Represent MSAT function at quality operations meetings • Create datasets using JMP or similar software • Establish operating ranges to support manufacturing activities
• 7+ years with BS/BA; 5+ years with MS/MA; 2+ years with PhD • Excellent verbal and written communication skills and superior organizational and project management skillset • Outstanding technical writing skills. Experience with CMC lifecycle and regulatory requirement • Must have worked in manufacturing, quality or MSAT environment and has the capability of driving risk assessment • 8+ years working experience in GMP field • Experience of technical writing skill and understanding of regulatory guidelines
• Short-term incentive bonus opportunity • Equity-based long-term incentive program • 401(k) plan • Paid vacation and holidays; paid leaves • Health benefits including medical, prescription drug, dental, and vision coverage.
Apply Now