Validation Engineer - Life Sciences

OPERATIONS - ENGINEERING/PRODUCTION

CDIC

AKKODIS Belgium is looking for an experienced person in a pharmaceutical environment in the field of validation.

Vos responsabilités :

• Ensure the execution or review of the required pre-tests before starting the final implementation of new processes.
• Coordinate all GMP documentation required for change control management (VP - TCD - VSR - QAGMP authorisation - QAGMP approval - external quota documentation, etc.).
• Write or revise PQ validation protocols and reports and analyse the results during PQ runs.
• Ensure the planning of validations in partnership with the C&M/QA departments and production; ensure communication with the production team in order to have the raw materials/assemblies/ad hoc resources for the validation.
• Ensure the operational management of the technicians dedicated to validations.
• Ensure all deviations related to the implementation of the change are addressed.
• Ensure the follow-up of QC results for each validation cycle and ensure timely collection/transfer of approved local documents to the RA department to ensure timely submission.
• Ensure review of dossier preparation in partnership with QA prior to submission of dossier to authorities.

Votre profil :

• You have a master's degree in industrial biology/chemistry or an industrial pharmacist title.
• You have experience in project coordination in a pharmaceutical environment. A previous technical background is a plus.
• You have experience and technical skills in the pharmaceutical industry.
• You are fluent in French and English.

19/08/2025