Associate Director, Global Regulatory Affairs # 4809

The Associate Director, Global Regulatory Affairs supports the vision, and strategic direction for the company's global regulatory function. This role reports to the Vice President, Head of Regulatory and is accountable for driving regulatory strategy across all portfolios—with a focus on diagnostics and device commercialization—influencing external regulatory policy, and ensuring global compliance in alignment with corporate objectives. The Associate Director/Director partners closely with executive leadership to guide portfolio and business-critical decisions, supports the company by preparing materials and presentations required for high-level interactions with health authorities, and develops the next generation of regulatory leaders.

This is a hybrid role based in Washington, D.C. Our current flexible work arrangement policy requires that a minimum of 40%, or 16 hours, of your total work week be on-site. Your specific schedule, determined in collaboration with your manager, will align with the team and business needs and could exceed the 40% requirement for the site.