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Join Becton, Dickinson and Company (BD) as a Sr. Regulatory Affairs Specialist in Kuala Lumpur, Malaysia. This full-time role focuses on ensuring medical device compliance and market access for APM products across the SEA region through strategic regulatory submissions and stakeholder engagement.

Requirements

  • Minimum of 3-5 years of experience in Regulatory Affairs within the medical device industry.
  • Experience in preparing and submitting regulatory applications.
  • Excellent written and verbal communication skills.
  • Ability to work independently and as part of a cross-functional team.

Skills & Responsibilities

  • Regulatory Submissions: Prepare, compile, and submit regulatory applications and manage existing approvals for the SEA region.
  • Compliance & Review: Review and approve product labeling, promotional materials, and change control documents for regulatory compliance.
  • Regulatory Strategy: Monitor and interpret new SEA regulations, assess product changes, and develop regulatory strategies for new product introductions.
  • Stakeholder Engagement: Interface with distributors, consultants, and regulatory agencies during submissions, inquiries, and audits.
  • Potential transition routes: People from quality assurance, clinical affairs, or compliance roles may bring transferable regulatory knowledge, alongside meeting the medical device industry experience requirements.

Job description

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

The Sr. Regulatory Affairs Specialist at Becton, Dickinson and Company plays a crucial role in ensuring APM products comply with regulatory requirements in SEA. This position involves preparing, submitting, and maintaining regulatory submissions, as well as providing guidance to teams to facilitate product changes and market access.

Job Responsibilities:
* Prepare, compile, and submit regulatory applications for SEA region.
* Manage and maintain existing regulatory approvals, licenses, and registrations, ensuring timely renewals and updates.
* Review and approve product labeling, promotional materials, and change control documents for regulatory compliance.
* 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 SEA regulations, standards, and guidance documents relevant to BD products.
* Develop and implement regulatory strategies for new product introductions and existing product modifications.
* Maintain accurate and organized regulatory documentation and databases.

Job Qualifications:
* Minimum of 3-5 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 visit https://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

MYS Kuala Lumpur - Damansara Heights

Additional Locations

Work Shift

Apply now
BD

Sr. Regulatory Affairs Specialist

Kuala Lumpur
On-site

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