Informations générales
Date de parution
/08/2025
Métier
OPERATIONS - ENGINEERING/PRODUCTION
Intitulé du poste
Validation Engineer - Life Sciences - M/F/X
Contrat
CDIC
Temps de travail
Temps plein
Description de la mission
AKKODIS Belgium is looking for an experienced person in a pharmaceutical environment in the field of validation.
Your responsibilities :
- 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.
- Ensure the follow-up of QC results for each validation cycle. - 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.
Secteur Industriel
Life sciences
Profil
Your profile:
- 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.
Localisation du poste
Europe, Belgique, Wallonie
Lieu
Avenue Jules Bordet Bruxelles
Critères candidat
Niveau d'études minimum requis
5. Bac +3 / Bac +4
Spécialisation du diplôme
* Chimie / Biochimie / Pétrochimie
* Hygiène, Sécurité et Environnement (HSE)
* Pharmaceutique
* Gestion de Projet
* Qualité et gestion des risques
Niveau d'expérience
1 à 3 ans