The role serves as the primary liaison between local RA representatives, regional stakeholders, and global functions to ensure alignment on regulatory requirements
Job Summary
The role serves as the primary liaison between local RA representatives, regional stakeholders, and global functions to ensure alignment on regulatory requirements.
Candidates will lead the development of the regional RA structure in APAC (excluding China) to support market access and lifecycle compliance for hearing care devices.
Sonova offers a flexible hybrid working model, extensive training opportunities, and a commitment to building an inclusive culture where diverse backgrounds are valued.
Matching Summary
The role serves as the primary liaison between local RA representatives, regional stakeholders, and global functions to ensure alignment on regulatory requirements.
Skills & Requirements
Must-have
8+ years regulatory affairs experience
APAC medical device regulatory knowledge
Leadership of regional RA teams
Stakeholder management across global functions
Product lifecycle compliance oversight
Nice-to-have
Advanced qualification in Regulatory Affairs
Fluency in additional APAC languages
Experience with OTC and e-commerce channels
Culturally aware diplomatic communication
Matrix organization leadership experience
Key Requirements
University degree in Life Sciences or Engineering
8+ years experience in medical device regulatory affairs
Experience leading multi-country regulatory environments in APAC
Advanced qualification in Regulatory Affairs preferred