Oversee supplier quality activities for NPI and production, ensuring compliance with ISO 13485 and regulatory standards. Drive supplier qualification and performance management, collaborating cross-functionally to achieve quality objectives.

Manage supplier quality activities for NPI and manufacturing. Ensure compliance with regulatory standards and drive performance improvements while collaborating across teams to achieve quality assurance objectives in a regulated environment.

Join a team that's dedicated to transforming innovative ideas into impactful medical devices. Lead cross-functional engineering teams through complex projects from concept to commercialization, ensuring alignment and excellence in execution.

Drive quality improvement initiatives in medical device complaint management, overseeing investigations, maintaining regulatory compliance, and collaborating with cross-functional teams to ensure product safety and efficacy.

Unlock potential in medical device innovation through regulatory leadership. Drive compliance and approvals by collaborating with cross-functional teams to optimize strategies and influence successful product launches in this vital role.