Senior Manager, International Regulatory Affairs

Sonova Group

Valencia, CA, United States
$126,400pyr - $189,600pyr; bonus eligible; medical...
**
International regulatory strategies
Pre-market and post-market registrations
Global telecom and battery regulations
** Sonova Group is seeking a Senior Manager for International Regulatory Affairs based in Valencia, CA. The role involves developing and executing global regulatory strategies for medical devices and telecommunications, managing registrations, and leading cross-functional teams, with a focus on compliance and performance management. **

Job Summary

  • Develops, implements regulatory programs and manages/leads International pre-market and post-market registrations for medical devices, telecommunications and other products as applicable.
  • Leads and coaches teams, driving performance management, employee engagement, goal setting, and adherence to company policies while fostering a dynamic, improvement-focused work environment.
  • Prioritizes the well-being of employees and fosters an inclusive environment that promotes engagement and collaboration, offering flexibility and individualized time management.

Matching Summary

Match Score: 75

** Sonova Group is seeking a Senior Manager for International Regulatory Affairs based in Valencia, CA. The role involves developing and executing global regulatory strategies for medical devices and telecommunications, managing registrations, and leading cross-functional teams, with a focus on compliance and performance management. **

Salary

$126,400/yr - $189,600/yr; Bonus eligible; Medical, dental, vision coverage, 401k plan with company match, PTO, paid parental bonding leave

Skills & Requirements

Must-have

  • International regulatory strategies
  • Pre-market and post-market registrations
  • Global telecom and battery regulations
  • Cross-functional team leadership
  • Regulatory intelligence and guidance
  • Relationship building with authorities

Nice-to-have

  • Adaptable and self-motivated
  • Improvement-focused work environment
  • Quality-focused culture
  • Bilingual preferred

Key Requirements

  • Bachelor’s degree required
  • Minimum 10 years experience
  • At least 5 years in regulatory affairs
  • At least 4 years management experience
  • Class III medical device experience preferred
  • Proficiency in MS Office and database management
  • Fluent in English

Work Rights

Not specified

Tailored Resume

Cover Letter