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Qualified Person

MSI Pharma
Start date
30 Oct 2023
Closing date
29 Nov 2023

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Job Details

Job Description:

We are looking for a highly qualified and experienced individual to join our client in as a Qualified Person (QP) in Belgium. As a QP, you will play a crucial role in ensuring the quality, safety, and compliance of our pharmaceutical products in accordance with Belgian and European regulations. You will be responsible for certifying batches of medicinal products for release onto the market and ensuring that all necessary quality standards are met.


  • Batch Certification: Certify batches of medicinal products for release, ensuring compliance with Good Manufacturing Practice (GMP) and European Union regulations.
  • Quality Oversight: Monitor and maintain the quality of all pharmaceutical products throughout the manufacturing and distribution process.
  • Regulatory Compliance: Ensure compliance with Belgian and European regulations, providing guidance on quality, safety, and efficacy standards.
  • Documentation and Records: Maintain accurate and comprehensive records related to batch certifications, quality control, and regulatory compliance.
  • Collaboration: Collaborate with various departments, including manufacturing, quality control, and regulatory affairs, to resolve quality-related issues and improve processes.
  • Audit and Inspection: Participate in and lead internal and external audits, as well as inspections by regulatory authorities.
  • Continuous Improvement: Identify areas for process improvement, propose and implement changes to enhance the quality and efficiency of operations.
  • Training: Provide training to staff members involved in the manufacturing and quality control processes.


  • QP Status: Hold a valid Qualified Person (QP) status as per Belgian and European regulations.
  • Educational Background: A degree in pharmacy, chemistry, or a related field is preferred.
  • Experience: Significant experience in a pharmaceutical or biotech manufacturing environment, with a strong understanding of GMP and quality assurance.
  • Regulatory Knowledge: In-depth knowledge of Belgian and European pharmaceutical regulations.
  • Strong Communication: Excellent communication and interpersonal skills to interact effectively with cross-functional teams and regulatory authorities.
  • Attention to Detail: Strong attention to detail and a commitment to maintaining high-quality standards.


  • Proficiency in Dutch and English is required. Knowledge of French or German is an advantage.


Founded in 2011, MSI Pharma specialises in recruitment and talent acquisition for pharmaceutical, biotech and life sciences staff on a permanent and interim basis.

We work in partnership with leading global brands and have a presence in the UK, DACH region, and North America.

Company info
3rd Floor (East)
The Cottons Centre,
Hays Lane
United Kingdom

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