Titre du poste : Commissioning, Qualification & Validation Engineer Lieu : Toulouse Département : MSAT Type de contrat: CDI JOB ID: 14858 We’re excited to share this opportunity is part of the Sandoz acquisition of Just-Evotec Biologics
Freelance Cleaning & CSV Documentation Specialist – Pharmaceutical Manufacturing Strasbourg, France – 5 Days Onsite 6–12 Month Contract – ASAP Start I’m currently supporting a pharmaceutical organisation looking for an experienced Cleaning & CSV Documentation Specialist
Dans le cadre du développement de son activité, AKTEHOM recrute un(e) leader métier spécialisé(e) dans les sujets Data Integrity et validation des systèmes informatisés (VSI) / computerized system validation (CSV). Le poste peut être basé à Lille, Colmar ou Paris.
Jobgether in France seeks a CSV Lead to drive computer system validation and compliance across GMP environments. You will provide validation leadership for computerized manufacturing and laboratory systems throughout their full lifecycle, partnering with Quality, Engineering, Automation, IT/OT, and project stakeholders.
Cookie NoticeValidation CSV Expert GDIT R&D and Medical page is loaded# Validation CSV Expert GDIT R&D and Medicallocations: Paristime type: Full timeposted on: Posted Todayjob requisition id: R-21131 Title: Validation CSV Expert GDIT R&D and Medical Company: Ipsen
Ipsen is strengthening its R&D and Medical Digital & IT organization to ensure the highest standards of compliance, quality, and audit readiness across its digital ecosystem. We are looking for a Computer System Validation (CSV) Manager to act
ARTO in Lyon is looking for a CSV Consultant for a 12-month project. The ideal candidate has more than 8 years of experience in Computerized Systems Validation and proven validation experience with MES, WMS, or AVEVA System Platform solutions. Excellent English
Freelance Cleaning & CSV Documentation Specialist - Pharmaceutical Manufacturing Im currently supporting a pharmaceutical organisation looking for an experienced Cleaning & CSV Documentation Specialist to support a new equipment project at their manufacturing site in Strasbourg.
Looking for a CSV Consultant for a 12 month project near Lyon. The desired profile should meet the following criteria: More than 8 years of experience in Computerized Systems Validation (CSV); Proven experience with the validation of MES, WMS, or
Êtes‑vous prêt à rejoindre un leader mondial dans les domaines passionnants et dynamiques de lindustrie pharmaceutique et des dispositifs médicaux ? Le groupe PQE est à lavant‑garde de ces industries depuis 1998 , avec 40 filiales