Principal Device Engineer

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 ambitious for patients, accountable for impact, and committed 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 Principal Device Engineer role sits in GSK’s Device Development and Engineering team is a high-performing group of scientists and engineers charged with the development and industrialisation of GSK’s drug delivery devices and combination products. We operate across all modalities and are looking for an experienced Device Engineer to combine core engineering expertise with strong technical, project and matrix leadership to deliver robust, reliable and patient centric device platforms that enable GSK’s late-stage portfolio.

The role is to be based at GSK’s R&D site in Ware R&D, Hertfordshire (UK) and can offer flexible hybrid working. Occasional travel may also be required.

• Provide technical leadership during the development and industrialisation phase of drug delivery and combination product programmes.
• Collaborate with multi-disciplinary teams across the GSK network and external device development and supply partners.
• Work within the design control framework to develop and execute work packages that form the basis of platform based DDF and RMFs.
• Contribute to the authoring of device parts of global submissions (e.g. technical file, BLA / MAA) and agency interactions.

• A degree or equivalent in Mechanical Engineering, Biomedical Engineering or any related discipline.
• Significant experience in drug delivery devices and the development of combination products (covering respiratory and/or parenteral dosage forms).
• Experience with requirements management, design controls, risk management, verification, validation and testing (ISO 14971 and 13485).
• A good understanding of assembly, scale up and tech transfer to manufacturing.
• A good understanding of usability and human factors.
• Strong leadership, teamwork and project delivery skills.
• Clear written and verbal communication.

Closing Date for Applications – Thursday 15th October 2026

• CMC Strategy
• Data-Driven Decision Making
• Data Integrity
• Debate Moderation
• Digital Fluency
• GxP Regulations
• Lean Management
• Problem Solving
• Process Optimization
• Project Leadership
• Risk Awareness
• Scientific Writing
• Technology Transfer

Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines.

We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health ple and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

GSK is an Equal Opportunity…