• DE
  • EN
  • FR
AKKODIS Careers website: All vacancies
AKKODIS

Follow us

  •  

  • Home
  • Submit spontaneous application
  • Searches, alerts
  • Akkodis site
 

Log in Candidate area

I already have a candidate area

Log in to candidate area




Forgotten password?

Register Create candidate area

You don’t have a candidate area. Click here to create one.

 

You are here :  Home  ›  Job Opening list  ›  Vacancy details

Selection: 0 job opening(s)
AKKODIS Careers website: All vacancies
AKKODIS

Follow us

  •  

Menu Careers website AKKODIS

  • Home
  • Submit spontaneous application
  • Searches, alerts
  • Akkodis site
AKKODIS job opening search engine
View all vacancies
RSS and other feeds
Information

Validation Engineer - Pharmaceutical Sector

  • Send this job opening to a friend
  • Print details (new window)
  •  


Détail de l'offre

Informations générales

RECRUITMENT (logo)

Date de parution

25/01/2023

Description du poste

Métier

OPERATIONS - ENGINEERING/PRODUCTION

Intitulé du poste

Validation Engineer - Pharmaceutical Sector

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

Localisation du poste

Europe, Belgique, Wallonie

Lieu

Avenue Jules Bordet 168 1140 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


Other vacancies

You may be interested in these vacancies

Project Engineer Civil Works Service

Add this job opening to selection Project Engineer Civil Works Service (2025-33925)
  • OPERATIONS
  • CDIC
  • Brussels
  • 28/04/2025

Assistant Project Manager

Add this job opening to selection Assistant Project Manager (2025-33924)
  • OPERATIONS
  • CDIC
  • Brussels
  • 28/04/2025

Tecnico per coordinamento cantieri di bonifica (Ingegnere Ambientale)

Add this job opening to selection Tecnico per coordinamento cantieri di bonifica (Ingegnere Ambientale)  (2024-31145)
  • OPERATIONS
  • Permanent contract
  • Milano
  • 26/04/2025
  • Privacy policy and Terms of use
  • Cookies
  • Configure your cookies
  • Accessibility: partial compliance
  • Sitemap
Go to top