• Own delivery outcomes for a portfolio of Atlassian programs across the enterprise • Establish delivery governance, standards, and operating rhythms • Manage interdependencies, risks, and escalations across programs • Lead enterprise Atlassian transformations, including Server/Data Center to Cloud migrations • Drive platform standardization, simplification, and modernization • Ensure secure, compliant, and resilient Atlassian environments • Partner with senior IT and business leaders to align Atlassian capabilities with enterprise goals • Translate business requirements into delivery roadmaps and execution plans • Provide clear executive-level status, metrics, and insights • Lead and mentor program managers, architects, and delivery teams • Enable Agile, DevOps, and ITSM operating models using Atlassian tools • Promote adoption, change management, and continuous improvement • Define and track KPIs focused on adoption, performance, cost, and business impact • Ensure delivery success is measured by outcomes, not just tool implementation

• Develop and deliver phase-appropriate product understanding and control strategies using QbD framework and risk assessment • Support manufacture of clinical and commercial GMP DS throughout product lifecycle, including tech transfer, campaign analysis, and diagnostics • Author and review technical reports, master and executed batch records, working across internal team and with CDMO partners • Work closely with CDMO partners, providing technical oversight (including onsite Person in Plant support when required), and taking the lead in supporting investigations and resolving deviations • Analyze process and manufacturing data to understand and optimize process performance • Develop process characterization and PPQ strategies and documentation • Support regulatory activities including submissions and site inspections from preparation through execution • Liaise with DP, device development, and clinical supply chain as needed to ensure seamless end to end product delivery and robustness • Develop and maintain cost of good models that describe process and enable sensitivity analyses for process improvements • Collaborate closely with colleagues to ensure a seamless, highly integrated TechOps team • Author and review internal procedures, reports, and presentations, as needed

• Guide process development of protein production from lab-scale to tech transfer and GMP manufacture at CDMOs (including onsite support when required, such as Person in Plant, inspection support, etc.) • Analyze process and manufacturing data to understand and optimize process performance • Troubleshoot processes to identify root causes, propose corrective actions, and support resolution of deviations • Review and approve master and executed batch records; assist with investigations • Author and review internal procedures, reports, and presentations • Develop process characterization and validation strategies and documentation • Support regulatory activities including submissions and site inspections from preparation through execution • Liaise with DP, device development, and clinical supply chain as needed to ensure seamless end to end product delivery and robustness • Collaborate cross-functionally with Regulatory to author and support regulatory submissions (IND, IMPD, amendments, IB, BLA, etc.) • Develop phase-appropriate product understanding and control strategies using QbD framework • Create late-phase development strategy to support potential commercialization. • Collaborate closely with colleagues to ensure a seamless, highly integrated TechOps team • Along with other TechOps team members, help shape goals and strategic vision for the TechOps organization

• Guide process development of protein production from lab-scale to tech transfer and GMP manufacture at CDMOs (including onsite support when required, such as Person in Plant, inspection support, etc.) • Analyze process and manufacturing data to understand and optimize process performance • Troubleshoot processes to identify root causes, propose corrective actions, and support resolution of deviations • Review and approve master and executed batch records; assist with investigations • Author and review internal procedures, reports, and presentations • Develop process characterization and validation strategies and documentation • Liaise with DP, device development, and clinical supply chain as needed to ensure seamless end to end product delivery and robustness • Collaborate cross-functionally with Regulatory to author and support regulatory submissions (IND, IMPD, amendments, IB, BLA, etc.) • Develop phase-appropriate product understanding and control strategies using QbD framework • Create late-phase development strategy to support potential commercialization • Collaborate closely with colleagues to ensure a seamless, highly integrated TechOps team • Along with other TechOps team members, help shape goals and strategic vision for the TechOps organization