{"id":3802537,"url":"https://alion.io/job/takeda-pharmaceutical-tech-transfer-program-management-lead-asia","title":"Tech Transfer & Program Management Lead, Asia","company":{"id":5984,"name":"Takeda Pharmaceutical","domain":"takeda.com","url":"https://alion.io/company/takeda","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":88,"open_postings":67,"ghost_share":0,"stale_share":0.448,"repost_share":0.075,"time_to_fill_p50_days":26,"computed_at":"2026-11-11T05:49:22Z"}},"role":"Operations","role_family":"Operations","seniority":"lead","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Shanghai, China"],"countries":["CN"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GMP","optional":false}],"status":"live","first_seen_at":"2026-11-05T12:07:32Z","employer_posted_date":"2026-11-05","last_verified_at":"2026-11-11T18:14:12Z","board_verified":true,"closed_at":null,"days_open":6,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":6},"description":"By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.\nJob Description\nAbout the role:\nPlan and execute assigned technology transfers, lifecycle management projects, launch readiness activities, and strategic MSAT programs from initiation through implementation\nCoordinate cross-functional teams, maintain integrated plans, manage risks and issues, and deliver milestones with discipline and transparency\nConnect science, technical strategy, manufacturing readiness, quality, regulatory, supply chain, and execution to support reliable product supply and successful launches\nApply a role interchangeable across EU, US, and Asia TT&PM teams, adjusting only geography, portfolio, reporting line, and local stakeholder context as needed.\nHow you will contribute:\nLead planning and execution of assigned commercial, late-stage, or lifecycle transfers through integrated transfer plans, milestone tracking, action management, governance preparation, and readiness reviews\nMaintain integrated project plans, critical paths, dependencies, decision logs, risk registers, issue logs, and communication plans\nCoordinate MSAT, modality teams, sites, Quality, Regulatory, Supply Chain, Engineering, Development/PharmSci, external partners, and enabling functions, building trusted relationships and alignment on scope, timelines, roles, decision rights, and expectations\nIdentify, document, escalate, and drive mitigation of risks and issues affecting timelines, quality, supply, regulatory readiness, or business outcomes\nCoordinate Tech Transfer Plans, Tech Transfer Protocols, comparability/readiness materials, governance updates, action trackers, and closeout documentation using TT Standardization & Program Excellence templates\nSupport engineering runs, PPQ readiness, validation planning, regulatory filing readiness, site readiness, and post-transfer stabilization with accountable technical and quality functions\nProvide clear, concise, timely communications, status updates, escalation summaries, decision requests, and portfolio inputs\nPrepare and support program-level steering and operating committees, team meetings, stage gates, and readiness forums, escalating beyond program scope to the Regional Head/Lead\nApply standard TT&PM tools, templates, reporting mechanisms, and knowledge management practices, feeding lessons learned back to TT Standardization & Program Excellence rather than creating local variants\nSupport digital and data-enabled tool adoption to improve visibility, knowledge transfer, action tracking, risk management, and execution speed.\nMinimum Requirements/Qualifications:\nBachelor’s degree in engineering, pharmaceutical science, biotechnology, chemistry, biology, project management, or a related scientific/technical discipline; advanced degree or project management certification preferred. \n5-10+ years of relevant experience in pharmaceutical or biotechnology manufacturing, MSAT, CMC, process development, technology transfer, program management, quality, supply chain, or a related technical function. \nDemonstrated experience managing cross-functional projects or workstreams in a regulated/GMP environment. \nWorking knowledge of technology transfer, manufacturing readiness, validation/PPQ concepts, change control, risk management, regulatory/quality interfaces, and lifecycle management. \nStrong project management discipline, organization, follow-up, meeting facilitation, and action tracking. \nAbility to communicate clearly with technical teams, site teams, and senior stakeholders; ability to translate complexity into concise actions and decisions. \nStrong collaboration and influencing skills in a matrix environment; ability to drive progress without direct authority. \nGrowth mindset and willingness to adopt standard tools, digital practices, and continuous improvement approaches.\nLocations\nCHN - Shanghai - ManufacturingWorker Type\nEmployeeWorker 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