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.
• The anticipated base pay range for this position is : $79,000.00 - $127,650.00; Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Matching Summary

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours for an immediate family member, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours per calendar year, Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Key Requirements

• Bachelor's or equivalent degree in Biology, Biochemistry, Microbiology, Chemistry
• 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