This role involves leading the regulatory strategy for a cardiology medical device company, focusing on FDA, CE, and UKCA submissions, and ensuring compliance with international regulations. You will work closely with the senior team and regulatory bodies, driving the company's expansion into new markets.
This role involves conducting incoming and dimensional inspections of components and materials, completing FAI reports, and maintaining quality records. The position requires strong experience with inspection equipment, engineering drawings, and quality documentation in a regulated meditech environment.
The Compliance Engineer will be responsible for creating, reviewing, and maintaining regulatory and technical documentation to ensure products remain compliant and audit-ready. Key responsibilities include authoring technical files, supporting EU MDR and UK regulatory compliance, and assisting with Notified Body and external audit requirements.
This role involves leading the Clinical Method Development and Validation team, overseeing bioanalytical method delivery, and ensuring compliance with GLP standards. Responsibilities include optimizing analytical systems, managing a team, and driving continuous improvement in a cutting-edge research environment.
This role involves hands-on, multidisciplinary engineering to design and develop complex medical devices, working closely with a diverse team of specialists. The projects span multiple medical specialisms, including surgical robotics, but the role requires a broad interest in various device types and engineering challenges.
The Territory Manager role involves driving the growth of Medtronic's Sacral Neuromodulation (SNM) therapy portfolio in South West England. Responsibilities include developing territory account plans, building relationships with healthcare professionals, and supporting clinical procedures to improve patient access to therapy.
This role involves leading customer experience improvements for service and repair operations across the EMEA region. Responsibilities include analyzing customer feedback, driving cross-functional initiatives, and promoting a customer-centric culture. The role requires strong data analysis, project management, and stakeholder engagement skills.
The Product Definition Lead will drive the technical direction and product definition for complex medical device systems, manage a team of systems and requirements engineers, and support the engineering team with technical issue resolution. The role involves close collaboration with interdisciplinary teams to translate business and clinical needs into precise requirements.
This role involves designing and developing complex mechanical products, from concept to manufacture. Responsibilities include 3D CAD modelling, DFMA, prototyping, testing, and working with suppliers to bring electromechanical products to market.
The Quality Improvement Engineer will lead projects to reduce defects and improve process performance in a highly regulated manufacturing environment. Responsibilities include investigating quality issues, implementing corrective actions, and working with cross-functional teams to enhance quality standards and operational performance.
This role involves managing product quality issues, leading root cause investigations, and working with Engineering, Production, and Supply Chain to drive continuous improvement. Key responsibilities include structured problem-solving, supporting new product introductions, and monitoring quality performance measures.
This role involves leading medical device development projects from concept to manufacture, managing multidisciplinary teams, and building client relationships. The position requires significant experience in mechanical engineering, medical device development, and project leadership.
The Senior Regulatory Affairs Specialist leads and supports regulatory activities for medical devices, including strategy development, impact assessments, and submission preparation for the US and international markets. The role involves collaborating with project teams, regulatory authorities, and internal stakeholders to ensure compliance and efficiency in regulatory processes.
This role involves ensuring the quality and regulatory compliance of cloud and embedded software for medical devices, particularly in the context of organ perfusion technology. Responsibilities include developing and maintaining software documentation, risk management, and collaborating with cross-functional teams to meet stringent medical device standards.
Perform physical and analytical stability testing on medical devices and skincare products in a GMP/GLP-compliant laboratory environment. Generate, analyse, and report stability data, support shelf-life claims, and contribute to regulatory compliance and continuous improvement initiatives. Operate and maintain analytical instrumentation while ensuring adherence to quality standards and safety procedures.
As an Account Manager in Sports Medicine, you will drive strategic growth across key accounts in South Wales, Cheltenham, Gloucester, and Worcestershire. You will craft and execute plans to expand the footprint of focus brands, collaborate with teams, and engage senior stakeholders to deliver value-based solutions.
