Senior Regulatory Affairs Specialist - MedTech Global

BD, a global medical technology company, seeks a Staff Regulatory Affairs Specialist to lead regulatory activities for infusion devices. You will collaborate with QA, R&D, and Medical Affairs to ensure compliance with US FDA and EU MDR requirements.

The role demands independent project management and proactive regulatory risk mitigation. The candidate should have 5-7 years in regulatory affairs for medical devices, ISO 13485 experience, and strong communication skills for global teams.