Japan Regulatory Compliance Manager

Amgen Technology Pvt Ltd.

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Japan - Tokyo Until 9/19/2026 5+ years exp H-1B sponsor history First posted July 21, 2026 Last posted July 21, 2026
Job description

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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About this role

Summary

Manage pharmaceutical regulatory activities, compliance, submissions, and沟通with authorities in Japan.

Job title

Japan Regulatory Compliance Manager

Experience level

5+ years

Minimum experience

5+ years exp

Industry

healthcare

Location requirements

Japan - Tokyo; remote work not specified

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

PMD Actregulatory compliancecommunicationIT skillsdocument management

Preferred skills

Master’s degreeDoctoral degree

Specializations

pharmaceutical regulationclinical complianceGMPregulatory submissions
Locations

Structured locations inferred from the posting.

Tokyo, Japan

On-site City