Position: Associate

Job type: Full-time

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Job content

We are looking for a Product Compliance Specialist for our international client, specialized in the medical device industry, and located in the Geneva area.

Do you have solid experience in Medical Device? Do you have some experience in Compliance?

This position could be interesting for you.

Responsibilities
  • You will participate in the improvement of the quality product system in accordance with the regulations.
  • You record reports and conduct vigilance claims that are reported
  • You coordinate the overall post-market surveillance activity within the different departments concerned
  • You analyze the trends and implement corrective and preventive actions
  • You prepare vigilance declarations in order to validate them
  • You are answering the questions from the authorities
  • You will manage quality product projects
  • You carry out internal audits
  • You participate in product risk management
Profile
  • You are an engineer with knowledge of manufacturing processes in a medical device company.
  • You have a very good knowledge of ISO 13485 and MD European and American Regulations.
  • You are fluent in English and French.
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Deadline: 10-05-2024

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