Principal Medical Affairs

the makers of possible

BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

We are BD, one of the largest global medical technology companies in the world. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us.

The Principal, Medical Affairs role provides strategic medical/scientific support for the designated product platforms—integrating knowledge of business and functional priorities to address complex problems and non‑standard situations. As a key contributor in a complex environment, this position works independently with minimal guidance, sharing expertise as they represent Medical Affairs on Innovation and New Product Development Teams. The role is responsible for the medical strategy for assigned products, supporting the safety and efficacy of global product registration and sustained marketing.

This is achieved through active contribution to the design and analysis of clinical/pre‑clinical studies and collaboration with Clinical Affairs, R&D, and other teams such as evidence review and development of evidence generation plans aligned to the tailored needs of products and geographies. In coordination with Regulatory Affairs, the Principal, Medical Affairs role is responsible for creating and reviewing the clinical and non‑clinical support and data packages needed for regulatory submissions.

Working cross‑functionally is critical to developing integrated Medical Plans that support products from idea to retirement. Cross‑functional partners include program management, Clinical Affairs, R&D, marketing teams, Regulatory Affairs, and Quality.

• Bachelor’s degree in a Biological Sciences, Engineering, or Medical field required.
• A minimum of 4 years of experience in clinical, scientific research, medical writing, or biopharma/medical device industry or a combination of education and experience is required.
• Experience in high‑quality medical/technical troubleshooting, analysis, and impact assessment with excellent written and oral communication skills.

• Advanced degree in Biological Sciences, Engineering, or Medical preferred or equivalent experience.
• Experience with Investigational Device Exemption studies / PMA products is highly desirable.
• Experience in pre‑clinical research, development and execution of pre‑clinical models used for medical device development and evaluation, and knowledge of GLP standards and regulations is desirable.

USA: RI – Warwick

USA: IL – Vernon Hills

$ – $ USD Annual

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally‑protected characteristics.