Find a position that matches your potential.

Our client designs, develops and markets next generation medical devices. They are currently seeking a Director of Regulatory Affairs to join their team in the Pacific Northwest.

What’s in it for you…

• Well-established mid-sized medical device company
• Good company culture – everyone is passionate about what they do – focused on continuing education
• Leadership has a high standard for quality – three members of leadership have been QSMR
• High visibility role – lead US Regulatory Affairs team to next level – develop existing talent
• Opportunities to assist OUS & Clinical Regulatory Affairs teams
• Opportunity for role to expand and grow – make your mark

To be considered for an interview, the following experience/skills are desired:

• Bachelor’s degree in a Scientific, Engineering, or Healthcare related field
• 7+ years experience US regulatory affairs experience in an ISO13485, FDA regulated environment
• Proven experience with full process FDA submissions – 510k is a must
• Comprehensive knowledge of domestic regulations
• Excellent leadership and project management skills; must have the experience and ability to successfully mentor/train members of the US Regulatory Affairs team

Salary: $190K to $210K base plus bonus

If you experience technical difficulty while applying to the position, please email your resume directly to MedicalDeviceTeam@MRIGlobalMedDevice.com