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open role · workday:amgen

Japan Regulatory Compliance Manager

$AMGNTokyo· posted Jul 21, 2026
RegulatoryManager

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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skills Bork detected

PMDA (Japan)GMP
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