Job Summary

• The QC CRS Experienced Analyst is responsible for conducting biochemical and testing of drug substance, final product release and characterization samples, and critical reagent qualifications of cell and gene therapy products, including CAR-T.
• This role is responsible for performing and overseeing analytical release, maintaining GMP-compliant documentation, supporting method qualification/validation, and partnering with manufacturing, QA, and regulatory teams to ensure the safety, identity, purity, potency, and stability of clinical cell therapy materials.
• Employees are eligible for the Company’s consolidated retirement plan (pension) and savings plan (401(k)), and participation in the Company’s long-term incentive program.

Matching Summary

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: Pension, 401(k), Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Key Requirements

• Bachelor's degree in Biology, Biochemistry, Microbiology, Chemistry or related field
• 4–6 years of hands-on experience in cell therapy or biologics laboratories
• Direct CAR-T or T-cell processing experience
• Demonstrated experience with flow cytometry, qPCR/ddPCR, and cell-based assays
• Working knowledge of microbiological assays relevant to GMP
• Strong understanding of GMP/GLP principles
• Experience with QC documentation practices
• Familiarity with LIMS, ELN, or comparable laboratory data management systems

Work Rights