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Job Details

Quality Assurance GMP Compliance

Company: MSI Group Limited
Location: Belgium
Reference: VR -7732
Closing Date: 25 Feb 18
Type: Contract
Salary (£): Competitive

Job Summary:

Freelancing role - Belgium



My client science-led global healthcare company in Belgium are looking for an experience Quality Assurance consultant to join their manufacturing team and to manage QA activities related to one or more Quality Systems 

The assignment would be a daily rate assignment where the client expects the ideal candidate to be available within 4-6 weeks

Main Duties involved:

To provide support/or and oversight for QA activities related to one or more Quality systems (e.g. deviation treatment) within a Manufacturing Performance Unit.



  • Ensure support is provided to develop process documents that are in alignment with regulatory expectations and internal global policies and standards
  • Manage QA activities related to one or more Quality Systems
  • Support the development of transversal GxP Process:
  • Training Management
  • Documentation / Change / Deviation Management
  • Manage relationship with operations
  • Identify potential quality and compliance risks and help to manage these risks through the

existing quality systems.


Education / Required Experience & Knowledge:

  • PhD or Master in Sciences linked to Biotechnology/Vaccines development (Engineering,Bio- engineering, chemistry) or equivalent by experience.
  • GxP (Aseptic, validation, cGXP, GMP)
  • previous experience in QA in a pharmaceutical industry
  • Experience in GxP (Aseptic, validation, cGxP, GMP)
  • Strong communication skills (able to communicate with different levels within MPU)
  • English Good Knowledge
  • French Fluent (Both Written and Spoken)


Apply for this job: Quality Assurance GMP Compliance

Contact Information:

Address:  Head Office
3rd Floor East, Cottons Centre, 47/49 Hays Lane London SE1 2QE
Tel:  02079401985
Fax:  02079909763
Website:  Visit Our Web Site

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