Quality Assurance Senior Manager, External Supply Quality

Singapore Manufacturing - Tuas JOB ID: R-248609 LOCATION: Singapore Manufacturing - Tuas ; Singapore - Singapore WORK LOCATION TYPE: Flex Commuter / Hybrid DATE POSTED: Jul. 01, 2026 CATEGORY: Quality Quality Assurance Senior Manager (External Supply Quality)

Amgen Singapore Manufacturing

HOW MIGHT YOU DEFY IMAGINATION?

Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring a Quality Assurance Senior Manager (External Supply Quality) in Amgen Singapore Manufacturing.

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What you will do

Are you a strategic quality leader, ready to take on a high-impact role? In this position, you’ll lead quality oversight for Amgen Contract Manufacturing locations in India. You will have regional responsibilities across manufacturing sites and operate at the intersection of quality, innovation, and global collaboration to ensure reliable and quality supply of our products. This role will be located in Singapore and require occasional travel to contract manufacturing locations in India. A strong background in synthetics or peptide manufacturing is preferred for this role.

In this influential role, you will:

• Act as the quality lead for supplier relationships, ensuring performance through robust monitoring, technical site visits, and continuous improvement.
• Drive proactive quality management of suppliers, ensuring compliance with global GMP standards and Amgen’s high expectations.
• Provide quality oversight of new product introductions, tech transfers, and process qualification activities at the contract manufacturing site.
• Review and approve quality documentation, including master batch records, deviations, CAPAs, product complaints, and change controls, with a sharp eye for risk and compliance.
• Perform tactical batch disposition activities in support of lot release
• Negotiate Quality Agreement terms and conditions and ensure adherence.
• Act as a key quality partner to manufacturing, supply chain, process development, and other Amgen internal functions.
• Take the lead in cross-functional initiatives and continuous improvement projects to improve regional operations and daily tasks.
• Ensure inspection readiness for our contract manufacturing sites and internal Amgen records. Support management of audit/inspection commitments to completion. Represent Amgen at product-specific regulatory inspections of the contract manufacturing site.
• As needed, perform person in plant responsibilities during Amgen manufacturing campaigns or to support key process steps at the contract manufacturer.
• Role will require travel and onsite engagement with contract manufacturing sites.

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What we expect of you

Basic Qualifications

• Doctorate degree and 2 years of Quality and Compliance experience OR
• Master’s degree and 6 years of Quality and Compliance experience OR
• Bachelor’s degree and/or 8 years of Quality and Compliance experience
• Strong background in GMP compliance, with a focus on external manufacturing or materials management.
• Significant Quality and/or Manufacturing experience at commercial manufacturing facilities. Technical experience with synthetics or peptide manufacturing is a strong plus.
• Confident communicator who can build relationships across technical and cultural boundaries.
• Track record of driving change, improving systems, and mentoring others within Quality.
• Skilled in using risk based decision-making approaches.
• Experience with regulatory activities and variation management.
• Proven ab