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- Bachelors or Master ́s degree in Engineering / Science field
- Over 6 years of experience in Quality Management Systems in a Pharma or Medical Device industry
- Knowledge of ISO 13485, IVDR, 21 CFR Part 820 and 11
- Excellent Quality Documentation skills (Good Documentation Practices)
- Ability to work independently
- English Mandatory, German is beneficial It would be a plus if you also possess previous experience in:
- Electronic Documentation Management (GxP Tools, MS office)
- Exposure to Certification body / FDA audits At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow's science and technology. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond.
Senior analytiker - Feldkirchen-Westerham, Deutschland - Danaher
Beschreibung
Join a team where you can be heard, be supported, and always be yourself.Support or Conduct training on tool usage SMARTSOLVE, EDMS, MasterControl The essential requirements of the job include: