Documentation & Validation Engineer

• Responsible for the validation according to the current GMP guidelines for an automated control system.

• Writing commissioning and qualification tests based on user requirements and functional specifications.

• Executing tests in an accurate and GMP manner.

• Performing risk assessments § Point of contact for validation topics, both internal and external.

• Work in a project team, follow up on schedules and milestones.

• Bachelor or master in technical degree.

• At least 2 years relevant (pharmaceutical GMP environment) experience.

• Knowledge of office applications: Word, Excel, Outlook.

• Experience with GAMP5, 21CFR part 11 and computer system validation.

• Affinity with computerized systems, such as PLC, SCADA.

• Fluent in English and good knowledge of French and Dutch.

• Good analytical & communication skills.

• Willingness to travel (sporadically).

Our offer:

• A responsible and varied job in a motivated and successful team.

• Good primary and secondary working conditions.

• A pleasant and collegial working atmosphere.

• GSM.

• Company car.

What happens once your application is submitted?

You will receive an email when your application has been processed.

One of our Talent Acquisition partners will review and verify if your application meets the qualifications of the role.

If your application has been successfully verified, you will be invited to a first interview either virtually or face-to-face.

Usually after the second/third interview round we will make a decision.
Please do not hesitate to reach out to our team at any stage of your application.