Principal Device Engineer

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Global Technical Development (PTD) is an organization of over two thousand people globally that are integral for the mission of Roche to develop meaningful medicines for patients. Therefore, we actively collaborate and develop creative technical solutions to bridge early-stage, late-stage and commercial product needs. The mandate is to expertly deliver the pipeline and supply quality products to patients.

The Device Development department within Roche Technical Development is responsible for the development and support of drug delivery devices for the product portfolio. Our activities span a range of engineering disciplines from the requirements definition phase through to commercialization and marketed product support.

Device Engineering combines design, engineering, testing, and manufacturing to develop reliable and safe drug delivery devices that meet the needs of patients, healthcare providers and Health Authorities.

This hands‑on role drives engineering excellence by applying design controls, solving complex device engineering challenges, and providing strategic technical guidance to ensure robust product development and compliance.

In this role, you will engage in cross‑functional collaboration, particularly with Quality Assurance, Device MSAT, Regulatory Affairs, Pharmaceutical Development, Clinical, and Commercial teams.

• Serve as the Technical Project Lead or Subject Matter Expert to drive the robust development of combination products and medical devices, ensuring a seamless advancement into clinical phases and commercial market applications.
• Apply deep engineering expertise and strategic insights, establish robust technical product requirements and develop drug‑device combination product design solutions to assure devices maintain the required level of performance throughout the entire product lifecycle.

• Collaborate with external partners providing technical oversight on mechanical designs for combination products while ensuring high performance, design robustness and fostering innovation.
• Lead internal and external technical investigations to swiftly resolve complex, design‑related issues using structured problem‑solving methodologies.
• Author and manage comprehensive design control documentation - including Design Development Plans, User Requirements Specifications (URS), Design Inputs/Outputs, Verification/Validation Plans, conformity assessments, and risk management files.
• Navigate the global regulatory landscape to ensure all product designs and processes comply with industry standards, specifically ISO 13485, ISO 14971, and 21 CFR Part 820 (with an emphasis on 820.30 Design Controls).

• University degree (BSc or MSc) in engineering or a related technical discipline from an accredited institution.
• 10+ years of experience in mechanical engineering and drug delivery device development within pharma or highly regulated environments (cGxP, QSR).
• Hands‑on expertise in pen injector and autoinjector development throughout the entire product lifecycle.
• Strong background in container closure systems, specifically prefilled syringes and cartridges for parenteral drug delivery.
• Proven technical leadership and advanced problem‑solving capabilities in cross‑functional team environments.
• Solid understanding of materials science applied to drug delivery systems, with expertise in damage mechanisms, defect identification, and performance testing.
• Deep knowledge of regulations, industry standards, and guidance for combination products and medical devices on a global scale.
• Direct experience navigating Health Authority interactions and…