Lead quality management processes for medical devices, focusing on post-market quality assurance, data analysis, supplier management, and compliance with regulations.

The FP&A and Reporting Manager provides legal and compliance advice, manages contracts and compliance programs, and ensures understanding of regulations within the organization.

Lead reliability engineering for medical device design, conduct reliability tests, ensure compliance with standards, and collaborate with teams for innovative product development.

The Legal Manager supports business growth by providing legal advice, managing compliance, drafting contracts, and ensuring understanding of laws and regulations.

The Internal Audit Manager leads audit activities for the Japan site, ensuring compliance with US-SOX. Responsibilities include developing audit plans, evaluating controls, preparing reports, and mentoring teams.