Experienced Analyst

Johnson & Johnson Innovative Medicine

Malvern, Pennsylvania, United States of America
Base: $79,000.00 - $127,650.00; bonus/equity: elig...
Not specified
Analytical testing
Gmp-compliant documentation
Cell and gene therapy products
Johnson & Johnson Innovative Medicine is seeking an Experienced Analyst to conduct biochemical testing and quality control for cell and gene therapy products, particularly CAR-T. The ideal candidate will have extensive experience in a GMP laboratory, strong analytical skills, and a commitment to maintaining compliance and safety in a regulated environment

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.
  • 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

Match Score: 85

Johnson & Johnson Innovative Medicine is seeking an Experienced Analyst to conduct biochemical testing and quality control for cell and gene therapy products, particularly CAR-T. The ideal candidate will have extensive experience in a GMP laboratory, strong analytical skills, and a commitment to maintaining compliance and safety in a regulated environment.

Salary

Base: $79,000.00 - $127,650.00; Bonus/Equity: Eligible for 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

Skills & Requirements

Must-have

  • analytical testing
  • GMP-compliant documentation
  • cell and gene therapy products
  • CAR-T
  • ELISAs, qPCR, Flow Cytometry
  • viral vector handling

Nice-to-have

  • organizational leadership
  • quality mindset
  • continuous improvement
  • lean practices

Key Requirements

  • Bachelor's degree in Biology, Biochemistry, Microbiology, Chemistry
  • 4–6 years of hands-on experience
  • direct CAR-T or T-cell processing experience
  • experience with flow cytometry, qPCR/ddPCR, and cell-based assays
  • strong understanding of GMP/GLP principles
  • experience with QC documentation practices

Work Rights

Not specified

Tailored Resume

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