Global Regulatory Affairs Expert for Medical Devices

Vor 5 Tagen


Hannover, Niedersachsen, Deutschland Aristo Group Vollzeit

The Aristo Group is a project and personnel consulting firm specializing in the life sciences industry. We are currently seeking a highly skilled Global Regulatory Affairs Expert for Medical Devices to join our team in Hannover, Germany.

About the Role

This exciting opportunity involves executing and assisting with medical device registration for the European Economic Area (EMEA) and China. Key responsibilities include:

  • Executing and assisting internal regulatory review processes for product life cycles and product development to ensure compliance with the Medical Device Regulation (MDR).
  • Supporting the evaluation of regulatory impact on current and new products.

To succeed in this role, you will possess a strong educational background in Engineering, Physics, Chemistry, Biology, or a related discipline, as well as 3+ years of experience in medical devices. Your expertise should include knowledge of applicable international regulations and standards.

We are looking for an expert who can drive change and innovation in regulatory affairs while working closely with cross-functional teams. If you have a passion for staying up-to-date with regulatory developments and can effectively communicate complex information, we would love to hear from you

Requirements
  • Dipl.-Bachelor's degree (BS) in Engineering, Physics, Chemistry, Biology, or a related discipline.
  • 3+ years of related experience in medical devices.
  • Knowledge of applicable international regulations and standards.

A competitive salary in the range of **€80,000 - €110,000** per year, depending on qualifications and experience, reflects the company's commitment to attracting top talent. The Aristo Group offers a dynamic work environment, opportunities for professional growth, and a chance to contribute to the success of a leading life sciences consulting firm.



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