Be part of something bigger at BD. Here, you’ll help us maintain our high standards from a regulatory perspective at all levels, with a keen focus on submissions. It requires acute attention to detail, excellent communication skills and a passion to keep learning and updating your knowledge, which we’ll help you do with regular learning opportunities. Here, you’ll use your in-depth knowledge of FDA, Canadian and ISO/MDD regulations and requirements surrounding medical devices to ultimately achieve a singular goal: advancing the world of health™. At BD, you can make a true difference of one.
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Job Type:
Full-Time -
Job Level:
Entry to Senior -
Travel:
Varies -
Salary:
Competitive -
Responsibilities
We are the people who give possibilities purpose
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.
Job Description
About the role
The Regulatory Affairs Specialist at Becton, Dickinson and Company plays a crucial role in ensuring APM products comply with regulatory requirements.
This position involves preparing, submitting, and maintaining regulatory submissions, as well as providing guidance to teams to facilitate market access.
Main responsibilities will include:
- Prepare, compile, and submit regulatory applications for META region.
- Manage and maintain existing regulatory approvals, licenses, and registrations, ensuring timely renewals and updates.
- Assess the regulatory impact of product changes and determine the need for new or updated submissions.
- Interface with distributors, consultants, and regulatory agencies during submissions, inquiries, and audits.
- Monitor and interpret new and evolving regulations, standards, and guidance documents relevant to BD APM products.
- Develop and implement regulatory strategies for new product introductions and existing product modifications.
- Maintain accurate and organized regulatory documentation and databases.
About you
- Minimum of 1-3 years of experience in Regulatory Affairs within the medical device.
- Experience in preparing and submitting regulatory applications
- Excellent written and verbal communication skills, with the ability to articulate complex regulatory requirements clearly.
- Ability to work independently and as part of a cross-functional team.
Why Join Us?
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 healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive.
We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face-to-face collaboration supports your learning, your progress, and your success.
To learn more about BD visithttps://bd.com/careers.
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.
Required Skills
Optional Skills
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Primary Work Location
ARE Dubai - Middle EastAdditional Locations
Work Shift
Success Profile
What makes a successful Regulatory Affairs Professional at BD? Check out the top traits we’re looking for and see if you have the right mix.
- Analytical
- Collaborative
- Communicator
- Persuasive
- Problem-solver
- Skilled presenter