Career CategoryInformation SystemsJob DescriptionHOW 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 innovative manufacturing capability and support services to deliver these therapies globally. Now we are hiring a Contract Development and Manufacturing Manager to support external manufacturing execution in India.Contract Development and Manufacturing ManagerWhat you will doThe Amgen Contract Development and Manufacturing (ACDM) Organization is seeking a highly qualified candidate to work with Amgen’s external network of development and manufacturing partners to ensure uninterrupted clinical and commercial supply for Amgen’s portfolio. The position will be in the TIDES business unit of ACDM and will focus on the late-phase clinical and commercial peptide manufacturing. This is a key role in a high-performing cross-functional, global organization and will support external process development, supplier relationship management, and oversight of manufacturing activities.The successful candidate will operate in a highly matrixed environment, driving cross-functional alignment and ensuring delivery across timelines, quality, and cost.Serve as program lead for external peptide manufacturing, accountable for end-to-end execution across development, clinical, and commercial stagesAct as a primary interface with CDMOs, working alongside the site lead to ensure alignment on program priorities and deliverablesDrive technology transfer, scale-up, and process readiness in collaboration with Process Development and site teamsProvide oversight of manufacturing activities to ensure readiness for GMP operationsIdentify and manage program risks (technical, supply, regulatory) and drive mitigation strategiesPartner cross-functionally (Process Development, Analytical, Quality, Supply Chain, Regulatory) to ensure integrated executionSupport sourcing and externalization activities including Scope of Work (SoW) development and supplier engagementEnsure adherence to cGMP requirements and Amgen business processes including deviations, change control, and investigationsMonitor and manage program performance across timeline, quality, and cost, escalating issues as neededPresent program updates, risks, and recommendations to senior managementOccasional domestic and international travelWinWhat we expect of youBasic QualificationsAny degree with 8-13 years of experiencePreferred QualificationsExperience leading external manufacturing programs at CDMOs, preferably in peptides or related modalitiesDemonstrated experience in technology transfer, scale-up, and GMP readinessStrong understanding of drug substance development through commercial manufacturingExperience working closely with manufacturing sites in a site-facing roleAbility to operate effectively in a matrixed, global organization with shared accountabilitiesStrong project leadership, stakeholder management, and communication skillsAbility to proactively identify and resolve complex technical and operational risks.