FlexaFlexa
  • Discover companies
  • Find a job
  • Resources
Sign inSign up

Quick links

  • Sign in
  • Sign up
  • Book a demo
  • Live feed

For employers

  • How Flexa can help
  • Case studies
  • Talent Insights Report 2026

For users

  • Discover companies
  • Find a job
  • Resources
  • The Flexa Awards

Flexa info

  • About us
  • Contact us
  • FAQs
  • Legal
FlexaFlexa

© 2026 Flexa, All rights reserved.

  • Privacy policy
  • Terms
Discover companies
Find a job
Resources
View company profileApply now

Working at BD

  • Company employees
    60,000+

Hiring in

  • Oceania
  • Central America
  • Northern America
  • Asia
  • Europe
  • Argentina
  • Brazil
  • Côte d’Ivoire
  • Chile
  • Dominican Republic
  • Egypt
  • Ghana
  • Nigeria
  • Puerto Rico
  • Senegal
  • South Africa

Office locations

Join BD as a Regulatory Affairs Specialist / Senior Specialist in Minato-ku, Tokyo, Japan. In this role, you will oversee the regulatory lifecycle of medical devices from development to post-market management, collaborating closely with global teams and the PMDA. This full-time position requires native-level Japanese and business-level English.

Requirements

  • Bachelor's degree or higher in a life science or related field.
  • Native-level Japanese and business-level English proficiency.
  • Preferred: 3+ years (Specialist) or 5+ years (Senior Specialist) of regulatory affairs experience in medical devices or pharmaceuticals.
  • Preferred: Knowledge of the Pharmaceutical and Medical Device Act, QMS ordinance, and PMDA negotiation experience.

Skills & Responsibilities

  • Regulatory Strategy & Submissions: Prepare and submit approval applications and QMS compliance documents for Class I to IV medical devices.
  • PMDA Negotiation: Communicate and negotiate with the PMDA and MHLW, handling inquiries effectively.
  • Project Management: Drive regulatory strategy from the early development stages and manage application schedules.
  • Cross-functional Collaboration: Partner with R&D, QA, and global teams to ensure compliance and market introduction.
  • Potential transition routes: People from R&D, product development, or QA roles may bring strong technical and analytical skills, alongside meeting mandatory language and life science degree 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

グローバルの最前線で生まれる医療技術を、日本市場へ。

薬事スペシャリスト/シニアスペシャリストとして、医療機器(クラスI〜IV)の承認戦略から上市後管理までを担い、製品ライフサイクル全体に関与いただくポジション。

申請業務にとどまらず、開発初期からプロジェクトに参画し、コンプライアンスを徹底しながら、事業戦略に沿った市場投入をリードしていただきます。

また本ポジションは、R&Dやプロダクト開発、QAで培った経験を薬事領域で活かしたい方にもオープンです。 リサーチの読解・理解から、論理的な整理・文書化に至る一連のスキルを基に専門性を広げていただけます。

職務内容

  • 医療機器(クラスI~IV)の薬事申請資料の作成・レビュー・提出
    (承認申請書、添付資料、QMS適合性調査申請書 等)

  • 独立行政法人医薬品医療機器総合機構(PMDA)および厚生労働省との折衝、照会事項対応

  • 製品開発段階からの薬事戦略立案および申請スケジュール管理

  • 上市後の薬事維持管理(軽微変更届、一変申請、定期報告 等)

  • 法規制の動向把握と社内への情報展開

  • SOPの整備、社内トレーニングの実施

  • 海外本社・グローバルチームとの連携

【必須/ Must】

  • ライフサイエンス系学部または関連分野における学士号以上。
  • 優れたコミュニケーション能力、交渉能力、プレゼンテーション能力。
  • 論理的思考力と問題解決能力。
  • 能動的かつ責任感を持って業務に取り組める方。
  • 日本語:ネイティブレベル、英語:ビジネスレベル

【歓迎(WANT)】

  • 医療機器または医薬品の薬事申請業務経験3年以上(スペシャリスト)または5年以上(シニアスペシャリスト)。
  • 薬機法、QMS省令、GCPなど、日本の医療機器関連法規制に関する深い知識。
  • PMDA/認証機関との折衝経験。
  • プロジェクトマネジメントスキル(シニアスペシャリストに求められる)。

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

.

Primary Work Location

JPN Tokyo - Minato-ku

Additional Locations

Work Shift

Apply now
BD

薬事(RA) スペシャリスト/シニアスペシャリスト

Tokyo
On-site

Similar jobs

Mars

Principal Scientist, Scientific and Regulatory Affairs

Chicago, Illinois
USD 119,040.00 - USD 163,680.00 / year
BD

Staff Specialist, Regulatory Affairs

Mississauga
$85,000 - $135,000 CAD Annual
BD

Staff Regulatory Affairs Specialist

Mississauga
$85,000 - $135,000 CAD Annual
BD

Staff Regulatory Affairs Specialist

San Diego
$129,600.00 - $207,400.00 USD Annual
Vodafone

Senior Regulatory Affairs Manager

London
Yearly bonus: 20%, Car allowance: £580-£630/month, Private pension up to 10% employer match
BD

Regulatory Affairs Coordinator II

Covington, Georgia