• Subject matter expert (SME) and process owner for Drug Product (DP) manufacturing of a small molecule used in non-sterile dosage forms • Oversee all technical drug product manufacturing aspects (fully under GMP) for a small molecule manufactured at an external manufacturer • Lead the technical workstreams of product transfers from development to commercial site and between commercial sites, scale-up activities, process validations and oversees manufacturing of Drug product with a small molecule at external manufacturers for projects in clinical and commercial phase • Lead internal activities related to external manufacturing such as process change assessments, major/critical deviations, risk assessments and CAPAs • Review and supervise set up, execution and documentation of DP related technical studies (CMC development and commercial operations), process and equipment qualifications and validations • Write and review applicable sections in registration files, variations and market expansion • Issue, review and approve applicable internal and external SOP's and external manufacturer manufacturing instructions • Contribute during set up of new analytical specifications and stability programs and review changes thereof • Support in sourcing evaluation of new Drug product small molecules, hard-gelatine capsule based alternative contract manufacturers and participation in developing supply and quality agreements • Be aware of external manufacturing technology advancements, understand and introduce new technologies and how they may be applicable to process innovation, cost or yield improvement

• Subject matter expert (SME) and process owner for Drug Product (DP) manufacturing of a small molecule used in non-sterile dosage forms. • Oversee all technical drug product manufacturing aspects (fully under GMP) for a small molecule manufactured at an external manufacturer. • Lead the technical workstreams of product transfers from development to commercial site and between commercial sites, scale-up activities, process validations and oversees manufacturing of Drug product with a small molecule at external manufacturers for projects in clinical and commercial phase. • Lead internal activities related to external manufacturing such as process change assessments, major/critical deviations, risk assessments and CAPAs • Review and supervise set up, execution and documentation of DP related technical studies (CMC development and commercial operations), process and equipment qualifications and validations. • Write and review applicable sections in registration files, variations and market expansion • Issue, review and approve applicable internal and external SOP's and external manufacturer manufacturing instructions. • Contribute during set up of new analytical specifications and stability programs and review changes thereof • Support in sourcing evaluation of new Drug product small molecules, hard-gelatine capsule based alternative contract manufacturers and participation in developing supply and quality agreements. • Be aware of external manufacturing technology advancements, understand and introduce new technologies and how they may be applicable to process innovation, cost or yield improvement

• Lead rapid development of MVPs for management portals, dashboards, and internal tools • Use AI-assisted development tools to prototype, test, and iterate quickly • Define product requirements, user flows, and data structures • Collaborate closely with engineering to deliver production-ready features • Gather and incorporate internal stakeholder feedback to refine tools • Help shape product direction for admin systems and operational tooling

• Spearhead the strategy and execution of next-generation products within the Retail Media ecosystem • Lead the "0-to-1" incubation of high-impact products • Define and drive a multi-year product vision • Identify whitespace and revenue opportunities • Partner with Data Science and Nielsen ONE teams • Define and execute an AI product strategy • Lead structured customer discovery • Oversee high-touch alpha/beta programs • Lead cross-functional squads to move from concept to MVP