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; Bonus/Equity: Eligible to participate in the Company’s long-term incentive program; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off.

Matching Summary

Salary

$79,000.00 - $127,650.00; Eligible to participate in the Company’s long-term incentive program; 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: 40 hours for an extended family member per calendar year, Caregiver Leave – 80 hours in a 52-week rolling period, Volunteer Leave – 32 hours per calendar year, Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Key Requirements

• Minimum 4–6 years of hands-on experience
• Bachelor’s or equivalent degree
• 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

Work Rights