Job Description Summary

Job Description

We are 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 MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Why join us?

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us!

About the role

The Regulatory Affairs Specialist plays a key role in ensuring compliance of promotional materials with regulatory standards across the EMEA region. As a member of EMEA Regulatory Business Solutions team, you will support the review and approval of promotional content, manage technical documentation, and drive continuous improvement initiatives within regulatory processes.

Main responsibilities will include:

• Regulatory review and approval of promotional materials (Ad Prom)
• Conduct thorough regulatory reviews of promotional and advertising materials to ensure compliance with applicable laws, guidelines, and internal policies.
• Collaborate with cross-functional teams including Marketing, Medical Affairs, and Legal to facilitate timely approvals.
• Actively contribute to the development and implementation of best practices within the Ad Prom COE (Center of Excellence)
• Review and approve Technical Data Sheets (TDS) in alignment with product specifications and regulatory requirements.
• Ensure accuracy and consistency of technical documentation across platforms.

About you

• Bachelor’s degree in Life Sciences, Pharmacy, or a related healthcare field.
• Experience in regulatory affairs, preferably within the medical device or pharmaceutical industry.
• Excellent communication, organizational, and analytical skills.
• Proficiency in English; additional languages are a plus

Click on apply if this sounds like you!

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

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.

To learn more about BD visit: https://bd.com/careers

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