QC Analyst, CAR-T Biotech – GMP & Data Integrity

Johnson & Johnson Innovation; Antwerpen; On-site; EUR 50,000 - 70,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Well-being reimbursement

Insurance plans

Job summary

Johnson & Johnson is seeking a QC Analyst, CAR-T Biotech to perform quality control testing for final drug product release and stability, ensuring GMP-compliant laboratory practices. You will support data integrity, investigations, and documentation while contributing to a safe, compliant work environment.

The role involves reviewing data, maintaining SOPs, and participating in audits, with a focus on CAR-T related assays and biotech QC processes.

Qualifications

• Bachelor's degree in a Scientific discipline (or related field) is required.
• 2+ years in a cGMP Quality Control lab or similar regulated setting preferred.
• Experience with cellular and/or molecular analytical techniques (qPCR, flow cytometry, potency assays); CAR-T experience is desirable.

Responsibilities

• Perform analytical testing for final drug product release and stability per GMP procedures.
• Peer-review laboratory data for accuracy and compliance.
• Author and maintain SOPs, WIs, and QC protocols as SME.
• Support investigations, deviations, CAPAs, equipment qualification, calibration, and maintenance.
• Participate in audits, inspections, and cross-functional collaboration.
• Deliver training and promote a safe, compliant laboratory environment.

Skills

qPCR

Flow Cytometry

Potency Assays

CAR-T experience

GMP knowledge

SOP writing and QA support

MS Office

Education

Bachelor's degree in a Scientific discipline

Tools

Microsoft Excel

Job description

Johnson & Johnson is seeking a QC Analyst, CAR-T Biotech to perform quality control testing for final drug product release and stability, ensuring GMP-compliant laboratory practices. You will support data integrity, investigations, and documentation while contributing to a safe, compliant work environment.

The role involves reviewing data, maintaining SOPs, and participating in audits, with a focus on CAR-T related assays and biotech QC processes.