Qualification and Validation
Merial part of Boehringer Ingelheim.
Koropi, Athens, GR
πριν από 10 μέρες

Responsibilities :

  • Act as one of the CSV Subject Matter Experts for Koropi site and support the validation manager in the preparation of validation documents and execution of validation / qualification activities (URS / IQ / OQ / PQ).
  • Support the validation manager in preparation and follow-up of the Annual Site Validation Master Plan (VMP)
  • Execute periodic reviews for computerized systems of the Koropi site
  • Execute supplier qualification for suppliers of computerized systems
  • Support execution of Factory Acceptance Tests (FAT) and Site Acceptance Tests (SAT) activities for equipment and utilities of Koropi site
  • Requirements :

  • Technical / academic degree in Engineering, IT, Chemistry, Pharmaceutics or other Natural sciences
  • At least 1 year of working experience in the pharmaceutical industry in Engineering, IT, Production or Quality / CSV area in an international environment
  • Excellent command of the Greek and English language
  • Good Manufacturing Practices (GMP) understanding
  • Previous experience with SAP systems is a plus
  • Professional and goal oriented dealing with critical, complex situations
  • Strong interpersonal skills to deal with interfaces and production personnel with broad variety of professional background
  • Demonstrated ownership for your decisions and actions
  • Prioritize your work, and drive execution excellence through discipline and collaboration
  • Please note that only resumes and cover letter in English will be considered.

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