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 Specialist will be responsible for handling document compilation for registration, renewal, amendment, and variations of the MDS portfolio (Medication Delivery Solution); as well as respond to regulatory related tender and customer requests.

Additionally, they will support the MDS EMEA Regulatory Affairs Team for labeling compliance activities and change management. They will ensure that products & sites achieve and maintain regulatory compliance by registration and timely renewals & will be responsible for pre-market regulatory activities of MDS business unit within the region.

Main responsibilities will include:

• Coordinating the communication and RA (regulatory affairs) activities between the local RA, quality, RA platforms and business.
• Providing support for labeling compliance by compiling vital document & information and reviewing the device labeling when needed.
• Keeping track of the open submissions and projects, analyzing, and closing the gaps.
• Responding to customer RA requests by providing document and information and providing support for tender RA documentation.

About you

• Educated to Degree level in Life Science (e.g. Biology, Chemistry, or other disciplines)
• Ideally have an experience in Medical Devices sector.
• Strong communication skills in English.
• Self-motivated, ability to work independently & build strong relationships within cross-functional teams.
• Computer-savvy with excellent organizational ability & capability to manage multiple, dynamic projects simultaneously.

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

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