Analyst Quality Control

Johnson & Johnson UK

Raritan, New Jersey, United States of America
Base: $65,000.00 - $104,650.00; bonus/equity: not ...
On-site
Biochemical and microbiological testing
Gmp regulations compliance
Electronic systems for documentation
Johnson & Johnson is seeking a Quality Control Analyst for its CAR-T team in Raritan, NJ, to conduct testing of final product samples and ensure compliance with relevant standards and regulations. The ideal candidate should have a scientific background, relevant work experience, and expertise in cellular and molecular techniques

Job Summary

  • The QC Analyst is responsible for conducting biochemical, microbiological, and/or general testing of final product samples submitted to the QC laboratories.
  • Perform analytical testing and maintain a safe work environment in compliance with all applicable procedures, EHS, and GMP regulations.
  • This shift is going to be scheduled 4:00pm - 2:00am through Sunday - Wednesday.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Quality Control Analyst for its CAR-T team in Raritan, NJ, to conduct testing of final product samples and ensure compliance with relevant standards and regulations. The ideal candidate should have a scientific background, relevant work experience, and expertise in cellular and molecular techniques.

Salary

Base: $65,000.00 - $104,650.00; Bonus/Equity: Not specified; Benefits: Eligible for Company’s long-term incentive program, 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

  • Biochemical and microbiological testing
  • GMP regulations compliance
  • Electronic systems for documentation
  • Aseptic processing experience
  • cGMP regulations and GDP knowledge

Nice-to-have

  • Cell and/or Gene Therapy experience
  • Process Excellence tools knowledge
  • Compendial requirements understanding

Key Requirements

  • Bachelor's degree required
  • 2 years of relevant work experience
  • Experience with qPCR, Flow Cytometry, ELISA, Cell Culture, or Potency assays
  • Experience in Biopharmaceutical or Pharmaceutical industry
  • Experience with Quality Control document reviews

Work Rights

Not specified

Tailored Resume

Cover Letter