Overview
At a time when patient outcomes are shaping global regulations, the EMEA Regulatory Affairs team is helping to ensure speed to market for BD’s innovative medical technologies by having an acutely patient-centric mindset. The Regulatory Affairs function has moved from being a back-office service provider to become a key strategic business partner.
Our Regulatory Affairs team manages the regulatory life cycle of BD products for EMEA in partnership with our business unit, country, region, segment and corporate Regulatory Affairs teams. We have a deep focus on globalization, category innovation, advocacy and customer outcomes using an agile infrastructure that helps enable the BD business strategy in a constantly evolving regulatory environment and provides our team with the opportunity to better serve customers in an effective manner.
What does this mean for you?
Regulatory Affairs within BD encompasses a diverse range of specialties, from biomedical engineering and life sciences to regulation and commerce. As our greatest asset, this means you can look forward to a wide range of opportunities to develop and grow your career. BD is an exciting choice for Regulatory Affairs professionals who want to combine their technical and management skills with business acumen. Here, you’ll work across our global businesses and be part of a team with an incredible breadth of technical expertise and cultural diversity that collaborates to ensure we consistently exceed expectations and serve our customers and their patients in the best possible way.
