Brabant Wallon - CDI

#validation #process #cleaning #bioprocess #qualification #equipment #pharma #GMP #CDI #Brabantwallon

Are you interested in the pharmaceutical industry and putting your knowledge of validation to good use?

Our client is actively looking for a Process Validation to strengthen its activities. Our partner is active in the pharmaceutical sector.

What are your responsibilities?

As Process Validation, you are in charge to

• You perform Validation activities for processes (injectables and Bio Processes), systems, clean utilities, in compliance with GMP, hygiene and safety rules in accordance with the site's Validation Master Plan System.
• You develop the operational Q/V activities at the level of injectables units and Bio Pilot.
• You participate in projects as Validation SME.
• You guarantee the qualified and validated state of processes and systems.
• You cover all the pharma technical aspects of the qualification and validation activities of all the equipment and processes of the development and commercial entities: bioprocess (bio pilot), production, analytical development laboratory (utilities).

You are graduated as a Master degree in Science or Engineering. You have 4 years experience in validation and in GMP environment. An experience in cleaning validation and/or process validation is very mandatory. You fluently speak French and English.

A permanent contract is offered for this function with a salary package matching your skills & experience. The opportunity to develop your skills or to evolve within this company is also open.

You're interested in this job? We kindly invite you to apply directly on our website experis.be. Do you have questions? You can contact or 0478/90.63.68.