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BD (Becton, Dickinson and Company) Regulatory Affairs Specialist (Hybrid) in Erembodegem, Belgium

Job Description Summary

As a Regulatory Affairs Specialist at BD Benelux, you will be responsible for ensuring that our products align with relevant regulations and standards, enabling them to be marketed and sold in the Benelux market. You will work closely with cross-functional teams to support product launches, review promotional materials, update regulatory documents and monitor regulatory changes. This role is critical in ensuring that BD Benelux's products meet regulatory requirements and can be marketed and sold in compliance with regulations and standards. Join us in a diverse and inclusive environment where everyone feels welcomed, appreciated and respected.

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!

Main responsibilities will include:

  • Handling customers’ questions

  • Support to customer service for tenders

  • Support cross functional teams for products launches

  • Review of promotional materials in French and Dutch

  • Update of regulatory documents and internal databases

  • Monitoring of regulatory changes in Benelux

  • Participation to trade associations meeting

  • Attend internal meetings with EU Regulatory Affairs team or project teams

  • As a regulatory affairs specialist you will support BD Benelux in regulatory activities for the different products categories.

About you

  • Master degree in sciences or pharmacy or equivalent

  • Previous experience in regulatory affairs of 3 years at least ideally in medical devices or in vitro diagnostics area

  • Good communication skills verbal and written in Dutch and English (French is nice to have)

  • Ability to handle several projects in parallel and interact with several functions

  • Autonomy

  • Computer skills including the office pack

Click on apply if this sounds like you!

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

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

Primary Work Location

BEL Erembodegem - Dorp 86

Additional Locations

Work Shift

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of 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, or any other protected status.

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