Regulatory Affairs Specialist
ElektaJapan
Posted March 19, 2026
Full Time
About the Company
At Elekta, our outcome-driven and cost-efficient solutions provide lasting clinical difference and are developed through sustainable environmental, social and governance practices. We’ve been working openly and proactively with clinicians and our partners for almost half a century to advance precision radiation therapy and meet continuously evolving patient needs—no matter where they are in the world. To us, it's personal, and our global team of 4,700 employees combine passion, science, and imagination to profoundly change cancer care. We don’t just build technology, we build hope. Elekta is headquartered in Stockholm, Sweden, with offices in 120 countries and listed on Nasdaq Stockholm. Visit elekta.com to learn more.
Job Description
Regulatory Affairs Specialist position at Elekta, responsible for obtaining regulatory clearance to launch new products and maintaining regulatorily cleared products within legal in accordance with the Japanese Pharmaceuticals and Medical device law.
Requirements
- High school degree or equivalent
- Bachelor's degree in a relevant field, such as pharmacy, law, or healthcare
- At least 3-5 years of experience in regulatory affairs, medical devices or pharmaceutical industry
- Excellent communication, negotiation and problem-solving skills
Benefits
- Comprehensive health insurance
- Retirement plan
- Generous paid time off
