Quality and Specialized Process Manager

Il y a 2 mois


Brussels, Belgique Michael Page Temps plein

The successful candidate will have the following responsibilities :

  • Develop, implement, and maintain a robust quality management system
  • Conduct regular audits and inspections to ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant quality standards
  • Oversee and optimise specialise processes related to pharmaceutical product development, manufacturing, and distribution
  • Drive continuous improvement initiatives for specialise processes
  • Monitor and evaluate the effectiveness of specialised processes
  • Ensure compliance with all applicable regulatory requirements
  • Coordinate regulatory inspections and audits

The successful candidate will have the following qualifications:

  • Study degree in Pharmacy
  • Fluency in French is mandatory and good knowledge in Dutch
  • Extensive experience in pharmaceutical quality management, including roles with a focus on GMP and GLP
  • In-depth knowledge of pharmaceutical regulations and industry standards
  • Strong analytic and problem-solving skills, with the ability to apply a risk-based approach
  • Project management experience, including the ability to lead and implement process improvement initiative




As the successful candidate will have the following advantages:

  • A multi-faceted challenge in a successful local company
  • An inspiring working atmosphere in a stable company
  • A growing salary package including company car, insurances and extra legal advantages, flexibility (Min 1 day/week home working policy)
  • Long Term development opportunities

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