CAR-T Biotech QC Analyst — GMP Testing

Johnson & Johnson Innovative Medicine; Beerse; On-site; EUR 55,000 - 74,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Insurance plans

Recognition awards

Job summary

Johnson & Johnson Innovative Medicine in Beerse is seeking a QC Analyst for the CAR-T Europe program. You will perform analytical testing and ensure GMP-compliant operations to support CAR-T manufacturing and related labs.

Required are a bachelor’s degree in a scientific field and at least 2 years in a cGMP QC lab, plus experience with qPCR, flow cytometry, and potency assays. Weekend shifts may be needed.

Qualifications

• Bachelor’s degree in a scientific field required.
• At least two years in a cGMP QC lab environment.
• Knowledge of biological/biochemical analytical data.
• CAR-T related analytical technologies and aseptic techniques.
• Experience with qPCR, Flow Cytometry, and potency assays.
• Familiarity with compendial requirements (USP/EP/JP) preferred.
• Proficient in MS Office; strong written and oral communication.
• Weekend shift may be required for clinical/commercial demand.

Responsibilities

• Perform analytical testing in compliance with specifications and GMP.
• Maintain a safe, compliant laboratory environment.
• Peer review of laboratory data.
• Author and update SOPs, WIs, and protocols for daily lab operations.
• Support laboratory investigations and CAPAs.
• Assist in internal audits.
• Provide input at cross-laboratory QC meetings.

Skills

cGMP QC

CAR-T experience

qPCR

Flow cytometry

Potency assays

Aseptic techniques

Biochemical analysis

MS Office

Written & oral communication

Education

Bachelor’s degree in a Scientific or related field

Tools

Document Management System

Job description

Johnson & Johnson Innovative Medicine in Beerse is seeking a QC Analyst for the CAR-T Europe program. You will perform analytical testing and ensure GMP-compliant operations to support CAR-T manufacturing and related labs.

Required are a bachelor’s degree in a scientific field and at least 2 years in a cGMP QC lab, plus experience with qPCR, flow cytometry, and potency assays. Weekend shifts may be needed.