- Minneapolis, Minnesota, United States
- On-site
- Full-time · Senior
- $110K–$150K per year
- 5+ years
Lead and execute regulatory strategy for implantable neurostimulation therapy for obstructive sleep apnea, supporting global regulatory activities in the U.S. and EU.
Compensation
$110,000—$150,000 USD
Responsibilities
- Serve as a strategic regulatory partner to cross‑functional teams
- Assess regulatory impact for new product development and post‑market changes
- Develop and communicate regulatory pathway options
- Compile, prepare, review, and submit high‑quality regulatory submissions in the U.S. and EU
- Collaborate with subject matter experts to respond to regulatory authority questions
Requirements
- Bachelor's degree in engineering, life sciences, or related scientific discipline
- Nice to have: medical device industry experience
- Nice to have: quality
- Nice to have: engineering
- Nice to have: software regulated as a medical device