Teams at Enovis

The Associate Director will lead global product management for the hip portfolio, defining market requirements, setting product strategies, and collaborating with various teams to launch new products.

The Senior Regulatory Affairs Specialist will develop regulatory strategies and manage submissions for medical devices focused on orthopedic technology, ensuring compliance with relevant regulations and standards.

Responsible for ensuring compliance with quality assurance procedures, conducting audits, supporting product development, and authoring documentation, among other duties.