The Manager leads a team responsible for supporting product registrations, information management, and regulatory intelligence across Cochlear's global portfolios
Job Summary
The Manager leads a team responsible for supporting product registrations, information management, and regulatory intelligence across Cochlear's global portfolios.
This role ensures alignment of corporate planning with regional requirements in EMEA, Asia Pacific, Latin America, and North America.
Employees enjoy the opportunity to make a difference to people's lives by developing world-leading medical devices that help people hear.
Matching Summary
The Manager leads a team responsible for supporting product registrations, information management, and regulatory intelligence across Cochlear's global portfolios.
Skills & Requirements
Must-have
5-7+ years regulatory affairs experience
Medical device product development experience
Team leadership and coaching skills
Global regulatory requirements knowledge
Submission preparation and lifecycle management
Nice-to-have
Master's or doctorate in relevant field
RAC certification
Strong stakeholder relationship building
Experience with software development regulations
Key Requirements
Bachelor's degree in engineering, legal, scientific, or healthcare
Minimum 5-7+ years regulatory affairs experience
Proven track record managing high-performing teams