Senior QP – Quality & Batch Release Leader

MindCapture

Antwerpen

Sur place

EUR 90 000 - 130 000

Plein temps

Il y a 4 jours
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Avantages offerts par ce poste

Meal vouchers
Eco vouchers
Health insurance
Group insurance
Net expense allowance
Company car with charging or fuel card
Training and career development

Résumé du poste

MindCapture in Antwerp is seeking a Senior Quality & Compliance QA/QP to oversee quality and release processes for an assigned manufacturing area. You will review batch release dossiers and support regulatory submissions, releasing commercial and clinical lots within the ERP system.

The role emphasizes testing oversight, ensuring GMP compliance, and collaboration with QA, regulatory, and operations. On-site work with strong onboarding and ongoing professional development is offered.

Qualifications

  • Master of Industrial Pharmacy is required.
  • Valid QP number according to Belgian regulatory requirements is required.
  • 8–10 years of pharmaceutical industry experience is required.
  • Experience as a QP is a plus.
  • Knowledge of biotechnology processes is advantageous.
  • Fluent in Dutch and English.

Responsabilités

  • Act as the primary QP contact for an assigned manufacturing area.
  • Provide QP feedback to QA engineers and escalate deviations or changes.
  • Review and approve batch release dossiers.
  • Release commercial and clinical lots in the ERP system.
  • Review and approve Certificates of Analysis, deviations and Product Specifications Sheets.
  • Review and approve regulatory submissions and changes.

Connaissances

Quality oversight
Regulatory submissions
Batch release review
Communication across QA/ops/regulatory

Formation

Master of Industrial Pharmacy

Description du poste

MindCapture in Antwerp is seeking a Senior Quality & Compliance QA/QP to oversee quality and release processes for an assigned manufacturing area. You will review batch release dossiers and support regulatory submissions, releasing commercial and clinical lots within the ERP system.

The role emphasizes testing oversight, ensuring GMP compliance, and collaboration with QA, regulatory, and operations. On-site work with strong onboarding and ongoing professional development is offered.

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