Job Description

Job Description

This is a full time, permanent position. Working a flexible 37 hour week, Monday – Friday.

The purpose of this job within the Device Engineering group is to support the design control and risk management subject matter expertise application to medical device and combination product development programmes throughout the product lifecycle.

This will involve generation and review of design history file and risk management file components whilst interacting with cross functional development teams at all levels of the client’s organisation.

Job Responsibilities:

  • Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures.
  • Support and facilitation of effective risk management activities at external design companies and manufacturing fa...

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