Quality Control (QC) Associate I (Cell and Gene Therapy)

Location: On-site in Torrey Pines, San Diego, California; relocation is not available.

Salary: $28.00–$33.00 annually for candidates working in San Diego.

Company

Develops iPSC-derived autologous cell replacement therapies for patients with high unmet medical needs, beginning with Parkinson’s disease.

What you will do

• Perform raw material inspection, sampling, and testing.
• Conduct environmental monitoring in aseptic manufacturing environments, including particulate, air, surface, and personnel monitoring.
• Test raw materials, intermediates, drug products, and stability samples according to approved protocols.
• Submit samples to contract testing laboratories and help organize QC laboratory operations and equipment calibration.
• Prepare cGMP-compliant testing data and reports.
• Participate in investigations of laboratory deviations and out-of-specification results.

Requirements

• Bachelor’s degree in Biology, Cell Biology, Microbiology, Molecular Biology, Biochemistry, or equivalent relevant education and experience.
• Laboratory experience in an academic or industry setting; experience in a cGMP-regulated environment is preferred.
• Basic knowledge of GMP regulations and applicable quality standards.
• Strong attention to detail, organization, communication, initiative, and ability to work both independently and collaboratively.
• Proficiency with Microsoft Office and other Microsoft applications.
• Valid U.S. work authorization without current or future employer sponsorship is required.

Culture & Benefits

• Collaborative, learning-focused work environment.
• On-site office and laboratory work, including possible extended periods in a cleanroom.
• Flexible availability for occasional weekend and holiday work to support production.
• Medical and dental insurance, paid time off, company-observed holidays, an on-site gym, and wellness benefits.
• Work may involve exposure to toxic or caustic chemicals and physical laboratory activities.