hirly

Stryker

Manager, Orthopaedics, Regulatory Affairs

Tokyo, Japan

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Stryker first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included

Matched against 2.4M live jobs from 200,000+ employers in 200+ countries.

Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Lead / management
Country
JP
Work mode
On-site / unstated
First seen by hirly
27 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Work Flexibility: Hybrid or Onsite

The Job's Mission

Under minimum supervision by Manager, he/she understands the related laws and regulations, and efficiently conducts the duties such approval applications, notifications and other related tasks.

マネジャーの最小の指導の下、薬機法全般に精通し、豊富な知識と経験を有し、円滑な薬事申請及び関連業務の遂行を目的とする。

Key Activities & Accountabilities

Responsibilities of this job is the appropriate execution of approval applications/notifications for medical devices which Stryker Japan K.K. manufactures and distribute. The duties are as follows:

Manufacturing and distribution/certification approval, notifications (including planning, collecting data, and PMDA/NB query correspondence)

Maintenance of approvals and certifications (Change control and periodical renewal)

QMS compliance inspection applications

Insurance listing applications (Creation of insurance listing application forms)

当社が製造販売する医療機器に係る下記を中心とした薬事申請業務の適切な履行を職責とする。

製造販売承認/認証申請、届出(計画立案、資料取集、PMDA/NB 照会対応)

承認/認証の維持管理業務(変更管理、定期更新)

QMS適合性調査申請

保険収載業務(保険適用希望書作成等)

Education

Language Skills (he/she is able to read and write English)

He/she has an ability to write the business documents

語学力(英語による文語でのコミュニケーションが実施できる。)

ビジネス文書を書くスキルがある。

Experience

6+ years of experience of medical device (Class I to IV) application approvals

Experience of PMDA consultation, and application approvals of improved device (preferably Class IV)

Good communications skills and project management skills

医療機器(クラスI~IV)の薬事申請における最低6年程度の実務経験

PMDA相談経験及び改良医療機器(クラスIVであれば望ましい)の薬事申請経験

コミュニケーションスキル、プロジェクトマネジメントスキル

Competencies

Not only high level of expertise required to the job, he/she needs to show a good communication skill in the organization. He/she can utilize the skill and communicate efficiently with internal related sections such as QC, WA, Sales & Marketing, Operations, Customer Care and etc.

He/she needs to have integrity and action-oriented mindset.

Please describe in detail the history of approval / certification application and the role you played in your resume.

業務に必要な専門性のみならず、組織の中で、円滑にコミュニケーションが取れる人材。社内関連部門(薬事、品質保証、品質管理、営業、マーケティング、オペレーション、カスタマーケア等)との良好かつ円滑なコミュニケーションが実施できる。

誠実な対応、率先して行動できる人材

職務経歴書に、承認・認証申請の履歴と担った役割を詳細に記載してください。

Travel Percentage: None

Original posting on Stryker's site ↗

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job
Manager, Orthopaedics – Stryker · Tokyo | hirly.me