
Global Regulatory Affairs Strategist - Medical Devices
Hyperfine, Guilford, CT, United States
A leading health technology company is seeking a Senior Regulatory Affairs Specialist in Guilford, CT or Palo Alto, CA. This hybrid role involves advising on regulatory strategy and ensuring compliance with domestic and international requirements for medical devices. The candidate should have a bachelor's degree and at least 8 years in the medical device industry, with a focus on regulatory affairs. Competitive compensation of $125,000 to $145,000 plus bonuses is offered, based on skills and experience.
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