CSV Engineer - Wavre - RealDev

L'ingénier CSV est responsable de la coordination et de la validation des systèmes informatisés et automatisu"es conformément aux exigences ręglementaires. · ...

En tant que consultant en Validation des Systèmes Informatisés (VSI), vous travaillez dans le département de contrôle qualité ou de R&D de notre partenaire afin de superviser et coordonner la stratégie de validation en collaboration avec les diverses parties prenantes (AQ, CQ, pr ...

Le rôle d'ingénieur CSV consiste à coordonner et à valider les systèmes informatisés et automatisés conformément aux exigences réglementaires, en garantissant leur conformité et leur fiabilité tout au long du cycle de vie du projet. · ...

Dans le cadre du démarrage d'une nouvelle zone de production pour l'un de nos clients du secteur pharmaceutique nous recherchons un(e) QA CSV pour renforcer l'équipe. Vos missions principales sont : · Mettre à jour le Master Plan de Validation et Qualification lié aux activités C ...

We are seeking a CSV Specialist to join our team in Brabant Wallon, Belgium. As a CSV Specialist, you will play a key role in ensuring compliance and integrity of computerized systems within a leading pharmaceutical environment. · ...

Role Overview · An exciting opportunity for a CSV Specialist to join a leading pharmaceutical company's Biological Drug Substance Business Unit, working on a pivotal CAPEX project aimed at doubling upstream capacity. Our client is seeking a proven professional to support qualific ...

I'm currently partnering with a global industry-leading pharmaceutical company that is expanding its manufacturing operations. · ...

As a center of excellence in technology innovation and project management the engineering department of our client in Puurs is working on the future of the site. · The ICS team within Puurs is working actively on the automation and integration of systems and data flows All these ...

Jouw Rol · Onze klant, een toonaangevende speler binnen de farmaceutische productie, versterkt zijn organisatie met een Junior CSV Engineer. In deze rol werk je binnen een hooggereguleerde GMP‑omgeving, waar kwaliteit, betrouwbaarheid en continue verbetering centraal staan. Je ma ...

· Jouw Rol · Onze klant, een toonaangevende speler binnen de farmaceutische productie, versterkt zijn organisatie met een Junior CSV Engineer. In deze rol werk je binnen een hooggereguleerde GMP‑omgeving, waar kwaliteit, betrouwbaarheid en continue verbetering centraal staan. Je ...

The CSV Specialist is responsible for the implementation, validation, and lifecycle management of a Manufacturing Execution System (MES) within a GMP-regulated pharmaceutical manufacturing environment. The role ensures that the MES is designed, configured, qualified, and maintain ...

The · CSV Specialist · is responsible for the implementation, validation, and lifecycle management of a Manufacturing Execution System (MES) within a GMP-regulated pharmaceutical manufacturing environment. The role ensures that the MES is designed, configured, qualified, and main ...

Join us for a career full of opportunities. Where you can make a difference. · ...

We are looking for a CSV Validation Specialist to develop and execute validation strategies for CSV projects. · ...

· Informations générales · Date de parution · /02/2026 · Métier · OPERATIONS - ENGINEERING/PRODUCTION · Intitulé du poste · Computerized Systems Validation Specialist - Life Sciences - M/F/X · Contrat · CDI · Temps de travail · Temps plein · Description de la mission · About Akk ...

Médiane Benelux: Career Booster · Since 2017, and with over 35 years of experience in France and Italy, Médiane Benelux is an engineering company specializing in software, electronics, and cybersecurity across key sectors such as Railways, Automotive, Energy, Medical, Aerospace, ...

We are seeking a Senior Automation Engineer to join a leading Life Sciences organization, · a current consultant role in industrial automation projects within regulated environments, · leveraging expertise in Systec tools and contributing to projects while ensuring compliance wit ...

We are seeking a Senior Automation Engineer to join a leading Life Sciences organization. · The role focuses on leveraging expertise in Systec tools and contributing to industrial automation projects within regulated environments. · ...

The Equipment Coordinator/TL coordinates laboratory equipment qualification and maintenance. · Maintain all QC laboratory equipment ensuring proper calibration qualification preventive maintenance according to schedule. · Oversee troubleshoot resolution of equipment related issue ...

We are seeking a Quality Assurance Specialist to lead quality assurance oversight for the implementation of automated systems within clinical laboratories. The ideal candidate will have experience in computerized systems validation (CSV) and equipment qualification. · Lead QA ove ...

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. · ...