Job ID R-548368 Date posted 06/24/2026

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.

  • Job Type:
    Full-Time
  • Job Level:
    Entry to Senior
  • Travel:
    Varies
  • Salary:
    Competitive
  • Glassdoor Reviews and Company Rating

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

Duties and Responsibilities

  • Support regulatory submission activities by preparing, organizing, and maintaining submission documents in alignment with local regulatory requirements.

  • Coordinate with internal teams (e.g., Marketing, Global RA, QA) to collect required information and ensure timely submission and approval tracking.

  • Monitor regulatory updates and assist in reviewing their impact on existing registrations and ongoing projects.

  • Track global and local registration status and maintain records in RIM systems, ensuring data accuracy and reporting support.

  • Assist in preparing responses to regulatory agency inquiries and support communication with relevant collaborators.

  • Support change management activities by monitoring notifications (e.g., NoC/ACR) and coordinating necessary license update actions.

  • Review promotional materials in Veeva Vault system to ensure regulatory compliance.

  • Provide general administrative and operational support for regulatory activities, as needed.

Qualification

Education and Experience

  • Bachelor’s degree in a science-based field such as Biomedical Engineering or related scientific fields.

  • Approximately 1 year of relevant regulatory or related experience preferred.

  • Experience in regulatory submission or documentation management is a plus.

Skills and Competencies

  • Good written and verbal communication skills (Korean and English).

  • Strong organizational and coordination skills with the ability to handle multiple tasks.

  • Basic understanding of processes and documentation requirements.

  • Proficiency in MS Office (Word, Excel, PowerPoint).

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

KOR South Korea - Seoul HQ

Additional Locations

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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

BENEFITS

Healthcare

Healthcare FSA

401(k)/
Retirement Plans

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Tuition Reimbursement

Paid Time Off

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Collaborative Culture

Competitive Compensation

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