We are seeking a Senior Design Assurance Engineer to support an expanding portfolio of medical devices as the organisation transitions from development to commercial scale. This role is central to ensuring product quality, regulatory compliance, and efficient design-to-manufacture transfer. You will work in a fast-paced environment, take ownership of key projects, and contribute directly to the development of life-changing healthcare products.Key ResponsibilitiesSupport and lead design verification and validation activitiesContribute to design controls, design reviews, and design change processesSupport regulatory documentation and submissionsDevelop and improve test methods, work instructions, and validation protocolsSupport human factors and usability studiesDrive corrective and preventive actions and root cause investigationsSupport design transfer from development to manufacturingExperience & QualificationsDegree (Level 8 or equivalent) in Engineering, Science, or related discipline3+ years' relevant engineering experienceExperience working within an ISO 13485 or similar regulated environmentStrong knowledge of design controls, FMEA, and medical device quality systemsFamiliarity with FDA and ISO regulatory requirementsExperience producing technical documentation and analysing dataPlease attach a copy of your CV.