Description

The Senior Manager of Quality Assurance at Amgen leads the QA department and plays a crucial role in establishing, implementing, and maintaining the Quality Management System. They ensure the organization’s compliance with regulatory standards and drive continuous improvement initiatives.

【Responsibilities】:

• Lead the QA department and play a crucial role in establishing, implementing, and maintaining Quality Management System.

• Establish drug GQP and QMS operating policies and organizational structure per Amgen GxP, Policies and Procedures, and government regulations- products may include sterile injectable monoclonal antibodies and proteins in vials, syringes and devices and small molecules in solid oral dosage form.

• Accountable for compliance with Amgen GxP, Policies and Procedures, and government regulations

• Confirm products to be dispositioned conform to applicable requirements including GQP ordinance requirements and perform disposition of products to Japan market.

• Manage GxP processes such as Batch Release, CAPA, Change Control Deviation, Self-inspection, Training, Complaint, Recall, Quality Agreement, Oversight on manufacturers etc.

• Contribute to Quality deliverables for Japan product launches, lifecycle events and other commercialization activities.

• Provide guidance and technical advice for PMDA Inspections that impact Amgen sites, as needed.

• Quality oversight of Contract Laboratories, Distributors and Logistic Service Providers as needed.

• Development and management of the GMP Intelligence Program to assess and monitor Japanese regulations, standards and guidance documents related to GxP, product testing and Japanese Pharmacopoeia requirements; as delegated, represent Amgen in key industry groups in Japan and provide Amgen stakeholders with guidance and interpretation on these requirements.

• Engage with global teams to promote a clear understanding of Japanese regulatory requirements, regulatory authority expectations, and customer expectations.

• Work with global teams to share good practices and to drive continuous improvement initiatives.

• Act as a deputy of Head of Japan Quality and Quality Assurance Supervisor if needed.

• Contribute to the Amgen K.K. (AKK) mission, vision and strategy.

【Basic Qualifications】

・Doctorate +2, Masters +4, Bachelors +5 years of directly related experience in quality assurance and quality related activities in a global commercial operation.

• Demonstrated ability to effectively manage a partnership alliance, including relationship development and maintenance, negotiation skills and oversight to monitor health of partnership.

【Preferred Qualifications】

Managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources

• Experience with Multi-National (MNC’s) as well as Japanese pharmaceutical companies

• Experience working with biologics (monoclonal antibodies and/or proteins) and small molecule solid oral dosage forms in Japan

• Experience with Investigational Medicinal Products (IMP) and commercial products

• Experience with combination products in Japan

• Preferred candidate either lived and or worked aboard.

• Flexible to travel

• Experience in GMP audits of laboratories that perform analytical testing of biologics, LSPs and manufacturing sites.

• Pharmaceutical/ Biologics product commercialization and lifecycle management experience

• Strong verbal and written communication skills in English and Japanese.

• Knowledge of regulatory authority inspection processes

Confidential Quality Assurance

• Experience in Japan with multiple language capability (English, Japanese)

• Strong verbal and written communications skills. Must be able to effectively articulate ideas with all levels of an organization.

• Self-leadership and motivation with high personal integrity and application of Amgen Values in daily operations.

• Must have demonstrated interpersonal skills, including temperament, objectivity and approach that will facilitate effective interactions with a team of seconded staff

• Ability for travel to international destinations as needed

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