Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects, Strategically drive as Component Lead for programs with complex supply chains having multiple manufacturing sites and secure global alignment among the different sites, Act as main interface to internal and external sites, Review technical documentation (protocols, reports) associated with manufacturing, tech transfer, site-to-site transfers and PPQ as needed, Manage and conduct scouting activities and recommend CDMOs for clinical and launch site selection from Tech Mgmt. Drug Product perspective, Create, communicate and implement technology transfer and manufacturing plans at the site which are aligned with crossfunctional CMC strategic discussions, Manage timelines, deliverables, and coordinate the input of technical and functional experts as needed, Communicates outcome of key meetings to stakeholders and functional areas, Cross-functionally drive technical recommendations for future sites and their selections, Collect and share key data from KPI perspective to improve Drug Product site performance, Conduct data review and analysis, data-driven decision-making process and support data transfer to the appropriate data repository, Recommend remediations, CAPAs and provide inspection support as appropriate to mitigate risks or gaps, Participate as the Drug Product component lead in the CMC working group meetings and communicate clear, timely and detailed updates on tech transfers and site activities, Support the compilation and technical review of relevant CMC sections of regulatory submissions, Coordinate with lab units, SC, RACMC, QA to drive collaboration and solve issues in Tech Mgmt. Drug Product team