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Amgen

Makes biotech medicines for serious illnesses

Quality Assurance Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeTokyo, JapanNo salary listed

About the Job

Requirements

  • A bachelor's or master's degree and at least 6 years of Quality and Compliance experience.
  • A strong background in good manufacturing practice (GMP) compliance, ideally focused on manufacturing or materials management.
  • Excellent written and oral communication skills in Japanese and English.
  • Quality and/or manufacturing experience at small- and/or large-molecule drug substance, drug product, and packaging manufacturing facilities.
  • Proven ability to lead audits, manage complex investigations, and influence quality improvements.
  • Skill in using risk-based decision-making approaches.
  • Experience with regulatory activities, variation management, and commercial product disposition requirements in Japan.
  • Experience with analytical testing situations, including method transfers, analytical qualifications, stability, laboratory investigations, in-process testing, and release testing.
  • A track record of driving change, improving systems, and mentoring others within Quality.

Responsibilities

  • Review and approve quality documentation, including master batch records, deviations, corrective and preventive actions, product complaints, and change controls, assessing risk and compliance.
  • Perform tactical batch disposition activities in support of lot release.
  • Negotiate Quality Agreement terms and conditions and ensure adherence.
  • Partner with manufacturing, supply chain, process development, and other internal functions on quality matters and build collaborative working relationships.
  • Lead cross-functional initiatives and continuous improvement projects to improve regional operations and daily tasks.
  • Ensure inspection readiness for contract manufacturing sites and internal records, support audit and inspection commitments through completion, and represent Amgen at product-specific regulatory inspections of contract manufacturing sites.
  • Lead supplier audits on behalf of Amgen for suppliers located in the JAPAC region.
  • As needed, perform person-in-plant responsibilities during Amgen manufacturing campaigns or to support key process steps at the contract manufacturer.
  • Provide quality oversight of new product introductions, technology transfers, and process qualification activities at contract manufacturing sites.
  • Drive proactive quality management of suppliers, ensuring compliance with global GMP standards and Amgen expectations.
  • Travel occasionally and engage onsite with contract manufacturing sites as needed.

Desired Qualifications

  • Manufacturing- or materials-management-focused GMP compliance background.
  • Quality and/or manufacturing experience at small- and/or large-molecule drug substance, drug product, and packaging manufacturing facilities.

About the Company

Amgen

Makes biotech medicines for serious illnesses

Amgen develops and makes biologic medicines, which are drugs built from proteins and antibodies grown in living cells, for serious conditions such as heart disease, cancer, and bone loss. Its anemia drug Epogen, approved in 1989, became one of the biotechnology industry's first blockbuster medicines. Amgen grows these drugs in large tanks called bioreactors, and its products include the cholesterol drug Repatha, the bone-building drug Evenity, and the severe asthma drug Tezspire. It earns money by selling these medicines, mostly through large drug wholesalers that supply hospitals and pharmacies. Amgen was founded in 1980 and is based in Thousand Oaks, California.

Company size
10,001+
Company stage
IPO
Headquarters
Thousand Oaks, CA
Founded
1980

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