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FDA Regulatory Affairs Director


Role Description

  • Line management, training of colleagues
  • Establish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements.
  • Training the team with EMEA / FDA requirements

Qualifications

  • Min 8 years in regulatory affairs in medical device
  • Min 4 years as Regulatory Affairs Manager
  • Experience with EMEA / FDA regulatory requirements
  • Ideally line management of a team
  • Excellent written and verbal in English & French
  • Availability to work 4 days in the office

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