Global Regulatory Affairs Specialist - Medical Devices & IVDR

Hero Recruitment is seeking a Regulatory Specialist for a full-time, permanent role reporting to the Regulatory Manager. You will help ensure all regulatory requirements are current across departments and support premarket submissions.

Responsibilities include maintaining technical documentation, handling regulatory reporting for CE-IVD products, and supporting audits. Collaborate with Quality and R&D to align regulatory activities with product milestones and market needs.