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The Associate Director leads regulatory affairs for Canada, ensuring compliance with local laws, guiding product registrations, and managing regulatory risks while collaborating with various stakeholders.

Conduct literature reviews, develop health economic models, analyze clinical trial data, create value communications, and support cross-functional teams for knees and spine products.

The Manager, Product Stewardship EPR will lead product stewardship and EPR regulatory activities, ensuring compliance with environmental regulations and supporting sustainable practices in product lifecycle management.

The Manager, Data Contracting Support oversees data contracting operations, ensuring compliance and effective management of data-related contracts with vendors and partners while collaborating with legal and business teams on privacy regulations.

The Manager of Compliance Risk Management oversees quality and compliance audits, focusing on compliance frameworks, risk management, and process improvements within the organization.

The Manager, Pre-Clinical & Clinical Compliance leads compliance activities for research programs, ensuring adherence to regulations and quality standards while managing risks and supporting audits.

The Director, Procurement Contracting leads procurement contracting activities, providing legal counsel and managing supplier contracts to ensure compliance, mitigate risks, and drive value in a regulated environment.

The role leads procurement activities for Joints-related categories, aligning category strategies with business goals and ensuring compliance while driving supplier performance and financial outcomes.

The Manager, CQ Site Lead is responsible for leading commercial quality processes and ensuring compliance with quality management standards at the West Palm Beach site.

The role involves leading MedTech sales, focusing on clinical sales for surgeons, with responsibilities in business development and team leadership.