• Your work will be split roughly 30/70 between product support within the team's ownership area — third-line tickets, performance incident investigation, and defect fixes — and building new platform features and optimizations. • You will own platform feature development end to end: technical design, implementation, merge procedures, and maintenance primarily on the web backend. • You will work with Business Analysts on detailed specifications and with QA engineers throughout delivery. • You will run peer reviews and hold the bar on technical design, code quality, maintainability, and performance.

• Provides strategic, technical, and architectural expertise to software development projects and team members. • Able to work independently with limited supervision in designing and developing new software products or major enhancements to existing software. • Acts at the highest level of technical expertise addressing problems on systems integration, and compatibility. • Performs feasibility assessments and often leads initiatives on development projects with other engineering staff. • Collaborates with Enterprise Architects and Project Management to translate design specifications to production platforms. • Designs, modifies, develops, and implements IT software architecture solutions. • Effectively plans and manages assignments spanning multiple complex projects. • Serves as a technical expert to IT Managers and functional teams in the IT organization. • Drives technical and procedural change relative to best practices in software development. • Champion and integrate AI-assisted development practices, including Agentic development, to enhance efficiency and product quality. • Builds teams as necessary to solve problems by taking ownership and mentoring developers in finding solutions. • Participates in the preparation, review, and analysis of software requirements and specifications. • Designs, plans, and coordinates work teams on new or existing software projects. • Provides guidance and expertise on sustaining or maintenance support to existing software. • Excellent communicator regarding technical issues with the ability to clearly define to senior management. • Defines and implements test strategies for software products. • Ensures compliance with internal policies, procedures and internal controls in accordance with the Sarbanes-Oxley Act 2002 Section 404.

• 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