PpAs the Global Head of Device Development, you are an enterprise leader and a key contributor to the One Pharma Strategy (OPS). You are responsible for the realization of the Device and Delivery Systems (DDS) strategy, ensuring Roche remains the industry benchmark for patient‑centric delivery technologies. You will lead a strong technical organization of over 120 scientific and engineering professionals with different experiences and backgrounds. /ph3Key Responsibilities /h3h31. Strategic Enterprise Leadership Portfolio Management /h3ulliShape the end‑to‑end platform strategy under DDS, from early‑stage design through industrialization and commercial lifecycle management to create maximum impact. /liliLead and support the company‑wide Technical Development (CMC) device portfolio, ensuring breadth and depth of technical capabilities, shared learning, and continuous improvement culture. /liliAct as the primary decision‑maker for development technology investments and platform selection in conjunction with PT device community leaders, chair the Global Device Review Forum (GDRF) and serve as a key member of the LSTDC for combination product topics. /liliPartner successfully with internal stakeholders to influence the external manufacturing network strategy, ensuring contract development and manufacturing organization (CDMO) partners are technically enabled to support patient‑centric delivery systems. /liliEnable “Design for Sustainability” principles of DDS, ensuring new device architectures are compatible with future environmental standards and circular economy initiatives. /li /ulh32. Device Community Architecture Influence /h3ulliLead the Global PT Device Community in a “Collective Leadership” model and collaborate deeply with Device and Packaging Industrialization (MSAT) teams, Pharmaceutical Development, Device Quality, and Regulatory to ensure an integrated approach to combination product health. /liliForge strong and reliable relationships with Head of RD units (gRED, pRED), Product Development, and Global Product Strategy to influence clinical development strategies and integrate device platforms early and effectively. /liliAct as an executive representative with Global Health Authorities and external strategic partners. /liliLead the external influencing agenda for combination product regulations and standards. /li /ulh33. Next‑Gen Innovation Technical Excellence /h3ulliAccelerate the development of the Next Generation of device platforms, including high‑volume Auto‑Injectors (3‑5mL), pen platform, and high‑volume delivery system. /liliEmbed Data, Digital, and AI capabilities into leadership and into device design. /liliTransition and further shape the organization toward a “Lab of the Future” model, utilizing predictive modeling and automated testing to accelerate design verifications and exceptional user experiences. /li /ulh34. Operational Excellence High‑Performing Organization (HPO) /h3ulliInstill a culture of technical rigor to eliminate operational friction and raise process efficiency, ensuring all foreseeable risks are identified early and mitigated with urgency (Right First Time). /liliDrive Lean/Operational Excellence principles to achieve productivity goals by leveraging platform knowledge and design histories. /liliActively motivate, mentor and develop “Ready Now” successors and rising stars. /liliFoster an inclusive environment reflecting Roche’s commitment to inclusion and belonging. /liliEmbody and role model Roche values and VACC (Visionary, Architect, Catalyst, Coach) leadership principles. /li /ulh3Who You Are /h3ulliAdvanced degree in Engineering (Mechanical, Biomedical, or Chemical), Life Sciences, or a related technical field is required. /liliExtensive years of experience in the medical device, Biotechnology, and Pharmaceutical industry, with several years leading large, complex technical organizations. /liliProven track record of navigating the complexities of CMC development from inception through commercialization. /liliDemonstrated ability to evolve systems, processes, or organizations to maximize impact. /liliBroad understanding of drug development, with specific expertise in combination products, human factors engineering, and design controls (21CFR Part4, ISO14971, ISO13485, MDR, and 21CFR820). /liliExceptional communication skills and demonstrated ability to influence at the senior executive level and build cross‑functional alignment across global boundaries. /liliExperience deploying digital tools, AI, or automated systems within a laboratory or manufacturing context. /lili25‑40% international travel required. /li /ulh3Leadership Competencies /h3ulliInspiring people leader passionate for leadership development; deeply experienced in leading through empowerment and accountability. /liliStrong ability to role‑model as a leader and to act as a coach and architect regarding system and process with clear accountability. /liliDeep experience translating complex technical hurdles into clear portfolio‑level business impacts for non‑technical senior stakeholders. /liliSavvy in prioritizing with the portfolio, business, and technical lens. /liliProven capability in navigating and managing ambiguity. /liliAbility to evolve system and processes to simplify at enterprise level. /liliProven track record in managing the business and performance of the organization. /liliAbility to engage in debate constructively with a solution‑oriented mindset; comfortable making high‑stakes decisions with urgency. /li /ulpWhere pay transparency applies, details are provided based on the primary posting location. For this role, the primary location is Basel. If you are interested in additional locations where the role may be available, we will provide the relevant compensation details later in the hiring process. /ppRoche is an Equal Opportunity Employer. /p /p #J-18808-Ljbffr