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Regulatory Compliance Specialist

vor 2 Monaten


Neuenburg, Neuenburg, Schweiz Masimo Vollzeit

Job Title: Medical Device Regulatory Affairs Specialist

Job Summary:

We are seeking a highly skilled Medical Device Regulatory Affairs Specialist to support registrations in the EMEA region. The ideal candidate will have fluency in English and knowledge of global medical device regulations.

  • Prepare country submissions and maintain regulatory certificates
  • Support registrations in the EMEA region
  • Collaborate with cross-functional teams to ensure regulatory compliance

Requirements:

• Fluency in English

• Knowledge of global medical device regulations

• Excellent communication and project management skills

• Ability to work in a fast-paced environment