QC CAR-T Investigation Lead – Weekend Shift (Beerse)

Biopharma Careers

Antwerpen

Hybrid

EUR 52,000 - 83,000

Full time

14 days+

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Benefits offered by this job

Annual bonus
Vacation days
Parental leave
Bereavement leave
Well-being reimbursement

Job summary

Johnson & Johnson in Beerse, Belgium, is seeking a QC CAR-T Investigation Coordinator for the Innovative Medicine Supply Chain Group. The role focuses on supporting daily QC operations and leading investigations related to CAR-T processes within a GMP framework.

The weekend team works Saturday and Sunday from 6:00 AM to 6:00 PM. Ideal candidates hold a Master’s in biochemistry or related field, with strong knowledge of cGMP and FDA/EU guidance, plus experience in GMP settings.

Qualifications

  • Master’s degree or Bachelor’s with relevant experience.
  • Knowledge of cGMP regulations and FDA/EU guidance is required.
  • Strong organizational skills and ability to work independently.
  • Excellent written and verbal communication skills.
  • GMP-regulated environment experience is an advantage.
  • Experience with molecular and cell biology techniques is beneficial.

Responsibilities

  • Support daily QC operations in collaboration with supervisors, analysts, Production, Warehouse, and QA.
  • Lead QC investigations and prepare final investigation reports with thorough root cause analysis.
  • Define and implement corrective actions; monitor effectiveness and ensure timely closure.
  • Coordinate cross-departmental QC investigations and act as QC representative.
  • Develop and deliver training or awareness sessions within QC.

Skills

GMP knowledge
Strong communication
Independent work

Education

Master’s degree in biochemistry/related field
Bachelor’s degree with relevant experience

Tools

PCR
Flow Cytometry
ELISA
Cell Culture
Mycoplasma testing
Microsoft Office

Job description

Johnson & Johnson in Beerse, Belgium, is seeking a QC CAR-T Investigation Coordinator for the Innovative Medicine Supply Chain Group. The role focuses on supporting daily QC operations and leading investigations related to CAR-T processes within a GMP framework.

The weekend team works Saturday and Sunday from 6:00 AM to 6:00 PM. Ideal candidates hold a Master’s in biochemistry or related field, with strong knowledge of cGMP and FDA/EU guidance, plus experience in GMP settings.

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