Weekend QC CAR-T Investigation Coordinator

7555-Janssen Pharmaceutica NV Legal Entity; Geel; Sur place; EUR 52 000 - 83 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Vacation days

Parental leave

Bereavement leave

Caregiver leave

Volunteer leave

Well-being reimbursement

Insurance plans

Résumé du poste

Johnson & Johnson is seeking a QC Investigation Coordinator for the CAR-T hub in Beerse, Belgium. This role supports daily QC operations and leads investigations, ensuring timely corrective actions within a GMP-regulated setting. Weekend hours from 6:00 AM to 6:00 PM are required.

Qualifications include a Master’s or Bachelor’s degree in biochemistry/biotechnology or related field, knowledge of cGMP and FDA/EU guidance, and strong communication skills. Proficiency in Microsoft Office is expected.

Qualifications

• Master's or Bachelor’s level degree with domain knowledge in biochemistry, biotechnology or related field.
• Experience with cGMP regulations and FDA/EU guidance is required.
• Strong organizational, written and verbal communication skills; ability to work independently.

Responsabilités

• Support daily QC operations with supervisors, analysts, Production, Warehouse, and QA.
• Lead QC investigations and prepare final investigation reports with root cause analysis.
• Define and implement corrective actions and monitor their effectiveness.
• Coordinate multidisciplinary teams for cross-departmental QC investigations and act as QC representative.

Connaissances

Strong organizational skills

Excellent written and verbal comun.

Independent work

Formation

Master's degree in biochemistry/biotechnology or related

Bachelor's degree with relevant experience

Outils

Microsoft Office

Description du poste

Johnson & Johnson is seeking a QC Investigation Coordinator for the CAR-T hub in Beerse, Belgium. This role supports daily QC operations and leads investigations, ensuring timely corrective actions within a GMP-regulated setting. Weekend hours from 6:00 AM to 6:00 PM are required.

Qualifications include a Master’s or Bachelor’s degree in biochemistry/biotechnology or related field, knowledge of cGMP and FDA/EU guidance, and strong communication skills. Proficiency in Microsoft Office is expected.