Quality and Specialized Process Manager - Brussels - FR/DU
Michael Page
- Bruxelles
- 60.000-80.000 €/an
- CDI
- Temps-plein
- 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, utilising data-driven insights and industry best practices.
- Monitor and evaluate the effectiveness of specialised processes, making recommendations for enhancements to meet quality and efficiency goals.
- Ensure compliance with all applicable regulatory requirements, including those set forth by health authorities and international regulatory bodies.
- Coordinate regulatory inspections and audits and ensure timely responses to findings and corrective actions.
- Bachelor's degree in pharmacy, chemistry, pharmaceutical sciences, or a related field; Master's degree preferred.
- 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 to quality management.
- Project management experience, including the ability to lead and implement process improvement initiatives.
- Relevant certifications such as Certified Quality Auditor (CQA) or Certified Manager of Quality/Organisational Excellence (CMQ/OE) are desirable.
- A multi-faceted challenge in a successful local company
- An inspiring working atmosphere in a stable company
- A growing salary package and extended package deal
- Self-development opportunities through internal job market as well as a wide range of training courses