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  • Location

    Brussels, Belgium

  • Job title:

    Validation Supervisor

  • Sector:

    Pharmaceutical

  • Job type:

    Permanent

  • Job ref:

    45559

  • Start Date:

    2021-03-01


Validation Supervisor - Quality Systems


The Company
Our client is a Belgian Biopharmaceutical company, specialized in the production of intermediates and finished products out of blood plasm. They are currently expanding their business and therefore we are looking for a Validation Supervisor - Quality Systems

Role Description
The Validation Supervisor will be responsible for everything regarding Validation within the plant. He/she will conduct Method Validation, Process Validation, Equipment Validation and CSV. Furthermore, the Validation Supervisor will coordinate a team of consultants on site.

Responsibilities

  • Conduct validations within production and QC labs
  • Writing and review of qualification/validation documents
  • Participate in improvement projects regarding validation
  • Maintain the GMP standards
  • Handling of CAPA's, risk assesments, change controls and deviations
  • Give training to other personnel regarding validation
  • Coordinate consultants on site during projects
     

Requirements

  • BSc. / MSc. Pharmacy in Life Sciences / Engineering
  • 3+ years of experience in validation
  • Extensive knowledge of GxP
  • Fluent in Dutch/English or French/English
  • Strong communication skills 
  • Experience with Trackwise is seen as an asset

Other information
My client is offering an undetermined contract with a good basic salary, topped up with attractive extra benefits (42 Holidays, Pension Plan, possibility for Company Car, Health Insurance, ...)

Contact Us

SIRE® LIFE SCIENCES B.V.

Staten Bolwerk 1
2011 MK Haarlem
The Netherlands
+31 (0) 20 658 9800

SIRE® STAFFING SOLUTIONS B.V.

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804