Regulatory Affairs and Quality Assurance Consultant Medical Devices

We want to expand our multi-functional team with a QA/RA professional with considerable experience in the Medical Device field to assist our medical device customers in meeting regulations and standards. Your tasks will include:

  • Help in the identification of regulatory requirements, including standards.
  • Assist in the interpretation of regulatory requirements and standards and translate them into practical specifications and project requirements
  • Guide customers through the entire regulatory process
  • Write or review procedures related to requirements of standards and regulations
  • Preferably also assist the customer with the implementation of a quality system in agreement with ISO13485.

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Interested? Please visit Randstad or send your CV and motivation letter directly to Inneke Teirbrood.

Regulatory Affairs and Quality Assurance Consultant Medical Devices
Regulatory Affairs and Quality Assurance Consultant Medical Devices