Job ID R-508800 Date posted February 12, 2025

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

Job Description Summary

Job Description

  • Support pharmaceutical and medical device customers for registration of new products and the license maintenance of existing products (including pre-fillable syringes).
  • Obtain the documentation and information necessary for registration in the targeted countries
  • Collaborate with Global RA Team Members to ensure timely execution of regulatory submissions with business objectives and customer deliverables.
  • Answer and fulfill requests and queries originating from regulatory authorities (MFDS, FDA, EU Notified body, Japan PMDA, China NMPA, Malaysia NPRA, etc.)
  • Identify applicable regulations and standards, carry out regulatory monitoring, assess the regulatory impact of changes, inform the appropriate internal and external stakeholders.

Job Requirements:

  • Pursue regulatory knowledge and expertise in countries regulatory topics
  • Minimum of 4-5 years regulatory or equivalent experience within a device or pharmaceutical company
  • Proactive, high performance, result oriented and manage projects with ethical integrity
  • Manage multiple projects and deadlines
  • Good verbal and writing English skill are preferred
  • Proficient in MS Office, including Word, Excel and PowerPoint

Veterans and persons with disabilities are given preferential treatment in accordance with relevant laws.

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

Advancing the world of health™

BD is one of the largest global medical technology companies in the world and is advancing the world of health™ by improving medical discovery, diagnostics and the delivery of care. BD helps customers enhance outcomes, lower costs, increase efficiencies, improve safety and expand access to health care.

At BD, we are committed to global inclusion and diversity. Increased inclusion and diversity drives innovation, allows us to better understand patient and customer needs, and ultimately makes BD the best possible place for all associates to thrive.


Brian Carney
Staff Regulatory Affairs Specialist

I love working with high powered leaders on a day to day basis who are respectful to my opinion and who I was never exposed to in my past job.


Robin Cassell
Global Regulatory Operations Labeling Specialist

I have been trusted in my ability to lead exciting and challenging projects with excellent upper management support. This in-turn has allowed me to grow and expand my regulatory knowledge that I believe will lay as a foundation to build my Regulatory career on.


Nikita A Mahendra Kumar
Senior Regulatory Affairs Specialist

BENEFITS

Healthcare

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Paid Time Off

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