{"id":429466,"url":"https://alion.io/job/amgen-contract-development-mfg-mgr","title":"Contract Development & Mfg Mgr","company":{"id":4775,"name":"Amgen","domain":"amgen.com","url":"https://alion.io/company/amgen","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":80,"open_postings":335,"ghost_share":0,"stale_share":0.773,"repost_share":0.018,"time_to_fill_p50_days":42,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"senior","employment_type":"contractor","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Hyderabad, India"],"countries":["IN"],"hiring_countries":["IN"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":8,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-07-21T00:00:00Z","employer_posted_date":"2026-07-21","last_verified_at":"2026-11-12T08:45:59Z","board_verified":true,"closed_at":null,"days_open":114,"trust":{"level":"ok","repost_count":0,"flags":[],"days_open":114},"description":"Career Category\nInformation SystemsJob Description\nHOW MIGHT YOU DEFY IMAGINATION?\nAmgen 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.\nContract Development and Manufacturing Manager\nWhat you will do\nThe 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.\nThe successful candidate will operate in a highly matrixed environment, driving cross-functional alignment and ensuring delivery across timelines, quality, and cost.\nServe as program lead for external peptide manufacturing, accountable for end-to-end execution across development, clinical, and commercial stages\nAct as a primary interface with CDMOs, working alongside the site lead to ensure alignment on program priorities and deliverables\nDrive technology transfer, scale-up, and process readiness in collaboration with Process Development and site teams\nProvide oversight of manufacturing activities to ensure readiness for GMP operations\nIdentify and manage program risks (technical, supply, regulatory) and drive mitigation strategies\nPartner cross-functionally (Process Development, Analytical, Quality, Supply Chain, Regulatory) to ensure integrated execution\nSupport sourcing and externalization activities including Scope of Work (SoW) development and supplier engagement\nEnsure adherence to cGMP requirements and Amgen business processes including deviations, change control, and investigations\nMonitor and manage program performance across timeline, quality, and cost, escalating issues as needed\nPresent program updates, risks, and recommendations to senior management\nOccasional domestic and international travel\nWin\nWhat we expect of you\nBasic Qualifications\nAny degree with 8-13 years of experience\nPreferred Qualifications\nExperience leading external manufacturing programs at CDMOs, preferably in peptides or related modalities\nDemonstrated experience in technology transfer, scale-up, and GMP readiness\nStrong understanding of drug substance development through commercial manufacturing\nExperience working closely with manufacturing sites in a site-facing role\nAbility to operate effectively in a matrixed, global organization with shared accountabilities\nStrong project leadership, stakeholder management, and communication skills\nAbility to proactively identify and resolve complex technical and operational risks\n.","description_format":"text","description_chars":3307,"description_truncated":false,"requirements":{"experience_years_min":8,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[{"name":"India","iso":"IN","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Prescription Drugs","Biologics & Biosimilars","Immunology & Inflammation Therapeutics","Cardiometabolic Therapeutics"],"lifecycle":[{"event":"open","at":"2026-09-06T05:38:59Z"}],"visa":[],"liveness":{"score":14,"band":"cold","label":"Long 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