Job Description
Job Summary: Regulatory Affairs Project Manager responsible for translating regulatory requirements into executable plans, leading cross-functional teams, and driving process improvements to ensure compliance with international regulations.
We are the makers of possible, a global medical technology company that advances the world of health. Our Purpose is to make a meaningful impact on people's lives, and we're looking for a talented Regulatory Affairs Project Manager to join our team.
Main Responsibilities:
- Translate regulatory requirements and strategy into executable plans at a level of detail that allows teams to understand what is critical at any one time
- Provide strong operational leadership to Regulatory and program teams, driving rapid and informed decision making
- Participate in the review of process/product changes, labelling, claims, product complaints, and A&Ps to determine the need for regulatory activities and ensure compliance to international requirements
- Drive process improvements and embed best practices from across programs and functions into supported teams
- Build value proposition through continuous refinement of delivery, prioritizing and focusing on areas of the highest impact and opportunity
About You: We're looking for a highly skilled Regulatory Affairs Project Manager with a degree in engineering or scientific discipline, and at least 5-7 years of experience in Medical Device Regulatory Affairs. You should have a strong understanding of the regulatory framework pertaining to Medical Devices, including pre-market regulations and risk management processes.
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer, committed to fostering an inclusive, growth-centered, and rewarding culture. We welcome individuals who can see the bigger picture, who understand the human story that underpins everything we do, and who are passionate about helping us reinvent the future of health.