Base: $81,992 to $122,989; bonus/equity: eligibili...
Hybrid (wednesday-saturday at santa monica, with occasional travel to tarzana)
Cgmp manufacturing
Cell therapy products
Aseptic techniques
AstraZeneca is seeking a Manufacturing Specialist for its Santa Monica location, focusing on cell therapy and cGMP compliance. The ideal candidate will have relevant experience in pharmaceutical or biotech manufacturing and will be responsible for ensuring operational readiness and tech transfer
Job Summary
The Manufacturing Specialist role will be responsible for ensuring successful manufacture and release of cell therapy products following all processes and procedures related to operations in full compliance with cGMP.
Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles.
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees.
Matching Summary
Match Score: 85
AstraZeneca is seeking a Manufacturing Specialist for its Santa Monica location, focusing on cell therapy and cGMP compliance. The ideal candidate will have relevant experience in pharmaceutical or biotech manufacturing and will be responsible for ensuring operational readiness and tech transfer.
Salary
Base: $81,992 to $122,989; Bonus/Equity: eligibility for various incentives, short-term incentive bonuses, equity-based awards; Benefits: qualified retirement programs, paid time off, health, dental, and vision coverage
Skills & Requirements
Must-have
cGMP manufacturing
cell therapy products
aseptic techniques
single use technologies
process validation protocols
Nice-to-have
operational excellence
Lean manufacturing principles
cross-functional initiatives
foster innovation
adapt to complex electronic systems
Key Requirements
2+ Years with BS/BA
1+ Years with MS/MA or Eng Degree
5 years' experience in pharmaceutical or biotech industry
clear understanding of cGMP process
knowledge of CMC regulatory framework for biologics
experience of aseptic techniques
experience supporting tech transfer
experience with GMP clinical/commercial manufacturing operations