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Regulatory Compliance Sr Engineer - Genève

  • A hirdetés 1127 napja lejárt
Description: Your role
  • You coordinate all aspects of the document development, control, review, revision, distribution, publishing and retention
  • You ensure all documents fully explain the associated processes, including any critical process parameters
  • You maintain and optimize the quality management system by assisting in strength and weakness analysis
  • You are in charge of the review and approval of processes, creates / revises procedures and work instructions to ensure these processes are correctly documented
  • You assist in Quality Planning projects and CAPA projects
Your profile
  • You hold a degree in business or engineering or professional experience in a similar position
  • You are familiar with a variety of office software packages including MS Word, Power Point, Visio, Excel, databases and SAP preferred
  • A significant knowledge / background in medical device industry is preferred
  • A sound knowledge of applicable ISO Standards, the Medical Device Directive 93/42/EEC and general knowledge of US Quality System Regulations is preferred
  • You have an excellent command of English and German both verbal and written
If you would like to hear more about this job then please don't hesitate to send your CV to or reach us out at . PS : Si vous souhaitez recevoir voir nos postes directement sur Linkedin, n'hésitez pas à nous suivre ! Link megjelenítése" width="0" height="0" />
Helyek Külföld
Kategória Külföldi munka
Aktiválás időpontja 2015.02.13.
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