Senior Vice President of Regulatory Affairs and Quality - Mechelen - Nipro Europe Group
About the Role
We are seeking an experienced professional to join our team as a Senior Vice President of Regulatory Affairs and Quality. The successful candidate will have a deep understanding of regulatory affairs and quality assurance principles, as well as experience working in the medical devices sector.
Key Accountabilities:
1. Manage, guide, and coach the RA Team to create and/or maintain compliance to applicable regulatory requirements.
2. Accountable for incident reporting to Competent Authorities.
3. Ensure the team meets regulatory requirements related to timely reporting, accurate, and comprehensive medical device reporting and follow-up.
Requirements:
1. University degree in a scientific field or equivalent by experience.
2. Strong experience in RA and QA departments within the Medical Devices sector.
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