Principal Regulatory Affairs Specialist - Global Operations jobs at Boston Scientific in United States, Minnesota, Arden Hills
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Company (1)
Job type
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Job title (1)
United States
Minnesota
Arden Hills
9 jobs found
09.05.2024
BS
Boston Scientific Principal Regulatory Affairs Specialist - Electrophysiology United States, Minnesota, Arden Hills
Develops domestic and international strategies for regulatory approval of Class I, II and III medical devices. Researches and advises company on country specific international product registration and compliance related requirements....
Supports the development of domestic and international strategies for regulatory approval of Class I, II and III medical devices. Coordinates, compiles, and submits U.S. and EU regulatory filings for new...
Advance scientific and educational objectives with appreciation of commercial landscape. Set strategy to partner with key opinion leaders in structural heart, interventional cardiology and electrophysiology on scientific and educational objectives....
Develops a deep understanding of customer needs and behaviors through market research, coordination with customer interfacing teams, internal and external data, as well as personal interactions with customers. Drives “Voice...
Creates novel technology enhancements to therapeutic ablation catheters to meet customer and market demands in the rapidly growing and evolving electrophysiology marketplace. Works with cross-functional engineering teams to develop prototype...
Support and manage applicable tools for pre and post market security testing; support integration of the tools into the quality processes. Support post-market activities to identify known/unknown vulnerabilities associated with...
Develop and execute innovative methods to source, evaluate, and pipeline external passive, diverse talent, and talent pools. Utilize tools such as Success Factors, Eightfold, social networking, competitive market intelligence, and...
Develops domestic and international strategies for regulatory approval of Class I, II and III medical devices. Researches and advises company on country specific international product registration and compliance related requirements....
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