• Define the technical strategy and long-term vision for projects built on the Skadina platform. • Provide leadership and mentorship to development teams, fostering innovation and best practices. • Ensure alignment between technical solutions and business goals. • Drive the adoption of Skadina across teams and promote a scalable architecture. • Oversee technical risk management and mitigation strategies. • Collaborate closely with stakeholders and architects to guide complex solution designs. • Ensure the platform is leveraged effectively to meet scalability, security, and performance goals.

• Subject matter expert (SME) for Small Molecules Drug Substance Manufacturing • Process owner of Small Molecules process validation for Sobi products • Lead and execute MSAT projects such as manufacturing process and cost improvement as part of LCM • Participate in internal activities related to (external) manufacturing, such as process changes, major/critical deviations, risk assessments, and CAPAs • Issue, review, and approve applicable internal and external SOP’s and manufacturing instructions • Review and supervise the setup, execution, and documentation of technical studies, qualifications, and validations • Write and review applicable sections of the APR/PQR • Write and review applicable sections in registration files, variations, and market expansion • Support in sourcing evaluation of new Small Molecules contract manufacturers and participation in developing supply and quality agreements • Lead the technical part of a product transfer, scale-up activities, validations, and oversee manufacturing of Small Molecules processes at external manufacturers for Sobi projects in the clinical and commercial phase • Be aware of external biopharmaceutical 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) for Small Molecules Drug Substance Manufacturing. • Process owner of Small Molecules process validation for Sobi products. • Lead and execute MSAT projects such as manufacturing process and cost improvement as part of LCM. • Participate in internal activities related to (external) manufacturing, such as process changes, major/critical deviations, risk assessments, and CAPAs. • Issue, review, and approve applicable internal and external SOP’s and manufacturing instructions. • Review and supervise the setup, execution, and documentation of technical studies, qualifications, and validations. • Write and review applicable sections of the APR/PQR. • Write and review applicable sections in registration files, variations, and market expansion. • Support in sourcing evaluation of new Small Molecules contract manufacturers and participation in developing supply and quality agreements. • Lead the technical part of a product transfer, scale-up activities, validations, and oversee manufacturing of Small Molecules processes at external manufacturers for Sobi projects in the clinical and commercial phase. • Be aware of external biopharmaceutical 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) for Small Molecules Drug Substance Manufacturing • Process owner of Small Molecules process validation for Sobi products • Lead and execute MSAT projects such as manufacturing process and cost improvement as part of LCM • Participate in internal activities related to (external) manufacturing, such as process changes, major/critical deviations, risk assessments, and CAPAs • Issue, review, and approve applicable internal and external SOP’s and manufacturing instructions • Review and supervise the setup, execution, and documentation of technical studies, qualifications, and validations • Write and review applicable sections of the APR/PQR • Write and review applicable sections in registration files, variations, and market expansion • Support in sourcing evaluation of new Small Molecules contract manufacturers and participation in developing supply and quality agreements • Lead the technical part of a product transfer, scale-up activities, validations, and oversee manufacturing of Small Molecules processes at external manufacturers for Sobi projects in the clinical and commercial phase • Be aware of external biopharmaceutical manufacturing technology advancements, understand and introduce new technologies, and how they may be applicable to process innovation, cost, or yield improvement