• Own and lead the end-to-end drug product development strategy, including pre-formulation, formulation development, scale-up, and clinical manufacturing. • Serve as the technical lead for all drug product activities with CDMOs, including selection, oversight and troubleshooting • Provide strategic guidance on raw material sourcing, manufacturability, product quality risk assessments, and lifecycle management considerations. • Identify and proactively mitigate technical, regulatory, and supply risks; develop contingency strategies to ensure program continuity. • Author, review, and approve drug product CMC sections for regulatory submissions (IND/CTA and amendments), and represent Drug Product CMC in regulatory agency interactions. • Lead technical due diligence efforts, including CDMO evaluation, proposal review, data integrity assessments, and master batch record approval. • Establish and implement robust experimental strategies, including design of experiments (DoE), to optimize formulation and process development. • Mentor and provide scientific leadership to internal team members and consultants; elevate organizational capabilities in drug product development. • Lead process readiness activities for Pre-Approval Inspections (PAIs), ensuring manufacturing processes, documentation, validation packages, and technology transfer records are inspection-ready and aligned with regulatory expectations

• Maximize the CEO’s productivity by protecting and optimizing his time. • Conduct in-depth research on business and technology topics using Gen AI, online resources, and other tools. • Engage professionally with C-level executives and navigate corporate communications effectively. • Create high-quality written content: posts, articles, e-books, and more. • Manage and grow social media accounts, professional networks, and memberships. • Drive lead generation via social media and targeted content distribution. • Attend online conferences/webinars and deliver concise, insightful summaries. • Negotiate with service providers and coordinate relevant services. • Apply advanced social media expertise to enhance brand visibility. • Use modern Gen AI tools, including for avatar-based video production. • Perform basic web vibe coding tasks when needed. • Maintain meticulous attention to detail, even on repetitive tasks.

• Design and train custom architectures that fuse multimodal inputs • Read the latest research papers and prototype solutions • Define the technical strategy on model selection • Conduct rigorous code reviews and mentor research engineers • Solve ambiguous problems with no existing solutions

• Contribute to the analytics strategy and roadmap by collaborating with business stakeholders across portfolio • Deliver analytics dashboards or tools that support pharmacovigilance and regulatory affairs • Utilize advanced analytics, machine learning, and artificial intelligence techniques • Ensure the accuracy, integrity, and security of data to meet compliance standards and regulatory requirements • Translate business questions from study teams into well-structured analyses with actionable recommendations • Act as a key point of contact and partner to product managers and business functions • Stay abreast of industry trends, emerging technologies, and best practices in data analytics and insights