Commissioning & Qualification Engineer
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About Akkodis
If the following job requirements and experience match your skills, please ensure you apply promptly.
Akkodis is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software & technology services, robotics, testing, simulations, data security, AI & data analytics. The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow.
Akkodis is part of the Adecco Group. Our Website: Akkodis
Contexte
Dans le cadre d'un projet industriel stratégique en Belgique visant à accroître les capacités de purification de plasma d'un site pharmaceutique de premier plan, Akkodis recherche un(e) Ingénieur Commissioning & Qualification .
Intégré(e) à une équipe projet en phase d'exécution et de mise en service, vous contribuerez à la coordination, au suivi et à la réalisation des activités de Commissioning, Qualification et Computer System Validation (CSV) sur des équipements et systèmes critiques dans un environnement GMP.
Votre rôle en tant qu'Ingénieur Validation C&Q :
- Participer aux activités de Commissioning & Qualification des nouvelles installations conformément aux exigences du projet.
- Assurer le suivi et la mise à jour du plan de Commissioning & Qualification.
- Réaliser les activités C&Q sur les équipements de process tels que les systèmes de chromatographie, centrifugeuses, cuves et lignes de remplissage aseptique.
- Rédiger, mettre à jour et maintenir la documentation CSV (VPP, SRA, FRP, DRA, etc.).
- Développer et exécuter les livrables CSV : Design Review, Design Qualification, protocoles IQ/OQ et rapports associés.
- Veiller à ce que les écarts et problématiques liés au Commissioning & Qualification soient correctement traités tout au long du cycle de vie du projet.
- Assurer un reporting régulier auprès du responsable CQV.
- Collaborer étroitement avec les équipes Engineering, Production et Qualité.
- Apporter un support aux utilisateurs dans l'utilisation de l'outil Kneat.
Profil
- Diplôme d'Ingénieur ou Master à orientation scientifique, pharmaceutique ou technique.
- Minimum 5 ans d'expérience en tant qu'Ingénieur CSV dans l'industrie pharmaceutique.
- Expérience confirmée en Computer System Validation (CSV).
- Bonne connaissance des systèmes :
- MES (Siemens Opcenter)
- DCS (Siemens PCS7)
- OSI PI System
- SCADA
- Connaissance des environnements réglementés GMP et des activités de qualification (IQ/OQ/PQ).
- Expérience avec l'outil Kneat est un atout.
- Excellente capacité d'adaptation et d'intégration dans un environnement projet dynamique.
- Esprit analytique, rigueur et autonomie.
- Approche proactive et orientée solutions. xlxgzvr
- Maîtrise du français et de l'anglais, à l'écrit comme à l'oral.
YAHIA CHERIF Anissa
Senior Talent Acquisition Specialist – AKKODIS
0493/31.25.81
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