Qualification/Validation Engineer

Our client, a pharmaceutical organisation, is looking for a Qualification/Validation Engineer to support their Injectable department.

Location: Brussels area, Belgium

Duration: 6 months

Mission Description:
Within the Injectable department, our client is looking for a Q&V Support to:
Write the qualification protocols
Support the qualification & validation of autoclave, tanks, filter integrity tester etc.
Ensure the good progress of qualification tests/trials

Mission responsibilities:
Qualification of equipment (eg autoclaves) in correspondence with GMP and EU/US regulations
Write protocols for qualification tests
Perform qualification tests and manage deviations (CAPA)
Support for production by updating/modifying the SOP's and forms
Interact with production operators to identify needs (is SOP/form clear? Is the SOP/form applied? If not, why?)
Take action to ensure quality in the production zone
Report to project leader

Specific professional/technical expertise and key skills required:

Language skills:
French, English

Experience in pharma sector (eg production, qualification/validation)
team player
ability to interact with different actors of different levels (managers, project leaders, production operators)
ability to manage deadlines
stress resistant
ability to work in an environment with legal constraints
Engineering background in production is nice to have

This is a fantastic opportunity not to be missed. Please apply now for more information.