Device Lead, Technology and Innovation

Posted Date:
Dec 19 2025

At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting‑edge technology to transform people’s lives. GSK fosters a culture of ambition for patients, accountability for impact, and commitment to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success.

We’re uniting science, technology, and talent to get ahead of disease together.

The Device Lead, Technology and Innovation will serve an important role in developing, networking, and executing our strategies that expand and advance the company’s ability to deliver innovative, robust, and competitive technologies in drug delivery and combination products across GSK’s asset pipelines and portfolio. The ideal candidate shall possess deep knowledge of device technology landscape, technical design/development regimen, and innovative and risk‑taking minds.

You will work across R&D, Commercial, Global Supply Chain and external partners to explore/ideate, assess, and de‑risk GSK’s next‑wave device technologies, which includes but is not limited to parenteral and respiratory drug deliveries. The direct experience in the development of respiratory drug delivery systems i.e. nebulizers, DPI, pMDI, and SMI is highly desirable. This role will sit in our Device Technology and Innovation group, and offer growth, visible impact on patient‑centric solutions, and alignment with GSK’s mission of uniting science, technology and talent to get ahead of disease together.

This position will be based at one of GSK’s R&D sites in Upper Providence, Pennsylvania (US), Waltham, Massachusetts (US) or Ware, Hertfordshire (UK) and is offered as a hybrid position with an expectation to be on‑site 23 days per week, and occasional travel may be required.

• Monitor and analyze external market trends, competitive landscape, and emerging technologies to ensure access to cutting‑edge drug delivery technologies which are strategic to delivery GSK pipeline.
• Lead specific pipeline asset‑based device technology exploration, assessment, and feasibility studies while engaging with Early Engagement and Device‑ability, Device Engineering, Primary Packaging, Formulation and Patient Insight Subject Matter Experts (SMEs).
• Define and deliver technology development plans, including scope, schedule, budget and milestones.
• Coordinate cross‑functional teams and external partners to progress design, prototyping, testing and manufacturability assessments.
• Identify technical risks and lead mitigation activities using test programs, simulation, technical deep dive, and project and functional governance reviews.
• Communicate results and recommendations clearly to stakeholders and senior leadership.
• Manage a network of external technologic partners and engineering vendors to help accelerate innovation and both build and expand GSK’s drug delivery device capability.
• Help drive an internal culture of innovation, including developing and curating a portfolio of problem statements across the portfolio, leading structured ideation sessions, and encouraging creativity.

• Bachelor’s degree in Mechanical, Biomedical, Chemical Engineering or a related technical field.
• 10 or more years of relevant industry experience in medical device drug-device combination development.
• Experience with parenteral delivery devices such as pre‑filled syringes, autoinjectors, and on‑body injectors.
• Experience leading technology assessments, feasibility studies, or early‑stage device programs.
• Experience with design and development of medical device from early concept to launch phases, preferably in the drug delivery space.
• Experience with regulatory requirements for parenteral or respiratory combination products (21 CFR Part 4 & 820, ISO 13485, 14971 & IEC 62366).
• Experience working with external partners, suppliers or contract manufacturers.
• Experience with regulatory…