Regulatory Affairs Specialist -Total Device Lifecycle- Brussels Job in Brussels, Brussels, Belgium

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Regulatory Affairs Specialist -Total Device Lifecycle- Brussels Job Description

Would you like to have a broad overview of the medical device lifecycle? Would you like to see clearly what impact your work has on the final result?

A global leader in medical devices is looking for a Regulatory Affairs Specialist to strengthen the EMEA Regulatory team. In this role, you will work closely with the engineers that develop the devices and will be involved in the project from pre- to post-marketing. Therefore, you will have a good helicopter overview and see the end-result of your work.

Profile:

• Master Degree in Engineering or another technical degree
• Minimum 1 year experience in Regulatory Affairs for the Medical Device or pharma industry
• Knowledge of the medical device directive
• Fluent in Dutch and English

Regulatory Affairs Specialist -Total Device Lifecycle- Brussels Application Information

http://www.aplitrak.com/?adid=YS5iYWVyZS4zOTM1Mi42MTI5QG5vbnN0b3BwaGFybWEuYXBsaXRyYWsuY29t

Regulatory Affairs Specialist -Total Device Lifecycle- Brussels Summary

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