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Japan Regulatory Compliance Manager

Amgen

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What regulatory roles keep asking for: Stakeholder management (22%) — counted across their open postings here.

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  1. Why do you want to join Amgen?
  2. What is a weakness you are working on, and how?
  3. Tell me about yourself, and why this role is the right next step.
  4. Tell me about a problem you solved at work that you are proud of.
  5. Tell me about a time you disagreed with your manager. What happened?

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Career Category Regulatory Job Description Group Purpose The Compliance Group is responsible for MAH business license, Three-supervisors’ committee (Sanyaku-kaigi), Foreign Manufacturer Accreditation/ Foreign Manufacturer Registration (FMA/FMR), periodic GMP inspection, and other activities to ensure compliance the Act on Pharmaceutical and Medical Device(PMD) Act. and to support the execution of the pharmaceutical business. Job Summary Support the operation of the Three Supervisors’ Committee (Sanyaku-kaigi) including preparation of materials and meeting documentation. Excuse MAH license management and regulatory compliance activities in accordance with the Pharmaceuticals and Medical Device (PMD) Act. Carry out FMA/FMR and GMP-related application and maintenance activities. Prepare regulatory submission materials and support communication with health authorities in coordination with internal functions. Key Activities Perform MAH-related tasks: preparation and documentation for the Three Supervisors’ Committee, SOP/document management, inspection readiness, and training support. Support FMA/FMR acquisition and renewal: application, registration, and communication with MHLW/PMDA. Contribute to GMP inspection preparation in collaboration with Quality team. Handle import certificates (Yakkan) via Nippon Automated Cargo and Port Consolidated System (NACCS) and export notifications in a timely manner. Conduct regulatory review of promotional and non-promotional materials in terms of applicable laws, regulations, and internal policies. Knowledge and Skills Practical knowledge of the PMD Act. Basic communication skills for interactions with health authorities (PMDA, etc.). English proficiency for document preparation and email communication. Basic IT skills (business applications, document management systems). Education & Experience (Basic) Bachelor’s degree (preferably in a scientific field). At least 5 years of pharmaceutical industry experience in regulatory-related activities. Education & Experience (Preferred) Master’s or Doctoral degree .

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Listed on workday · posted 2026-10-13. ApplySarthi collects openings and links to application pages; the role is advertised by Amgen, not by us.