Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing...
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing...
This role involves serving as a clinical expert in complex wound care, providing hands-on support and education to healthcare professionals across North Wales and the Midlands. The specialist will guide clinical decision-making, advocate for advanced wound therapies, and ensure effective use of products within community settings. It combines clinical expertise with field-based relationship management to improve patient outcomes.
This role involves serving as a clinical specialist for advanced wound care, providing hands-on support and education to healthcare professionals across North Wales and the Midlands. The specialist will guide clinical decision-making, deliver training, and ensure appropriate use of wound therapies within the community setting. Success requires combining nursing expertise with relationship-building to improve patient outcomes.
The Senior Clinical Trial Leader role involves planning and executing clinical trials for innovative medical devices, working closely with cross-functional teams, clinical sites, and external partners. The position focuses on advancing clinical research and ensuring quality and compliance in the development of medical devices that improve patient outcomes.
The Senior Analytical Monitor role involves conducting analytical monitoring activities for multiple clinical trials, ensuring compliance with regulations and company policies. Responsibilities include performing regular reviews, detecting issues early, and collaborating with Site Managers and Central Monitoring Managers to improve data reliability and site satisfaction.
Leads cross-functional clinical trial teams to deliver global trials on time, on budget, and in compliance with regulatory standards. Oversees end-to-end trial execution, including risk management, budget control, and inspection readiness. Works closely with R&D Quality and regulatory authorities to ensure adherence to global health guidelines and internal processes.
This role leads the operational execution of global clinical trials within Johnson & Johnson MedTech, ensuring trials are delivered on time, within budget, and in compliance with regulations. The Senior Manager oversees cross-functional teams, manages risks, ensures inspection readiness, and drives quality across trial lifecycles. The position plays a key role in advancing innovative medical treatments through structured, patient-focused clinical development.
This role involves supporting global trade compliance by reviewing export controls for medical technology products, ensuring adherence to UK, EU, and U.S. regulations. The analyst will classify items, screen transactions, and collaborate with supply chain and engineering teams to mitigate risks. It's an early-career position focused on building expertise in a highly regulated, international environment.
Leads environmental, health, safety, and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. Focuses on risk-based safety integration, incident investigation, and continuous improvement in highly regulated MedTech environments.
This role leads environmental, health, safety, and Process Safety Management (PSM) programs at a manufacturing site, ensuring regulatory compliance and driving a strong safety culture. The position acts as the site's PSM subject-matter expert, conducting hazard analyses, incident investigations, and risk mitigation in collaboration with operations and leadership. It focuses on continuous improvement of safety systems and fostering accountability across teams.
This role focuses on maintaining master data integrity across commercial systems, ensuring data accuracy, compliance, and consistency. The specialist will implement data governance practices, support MDM system implementations, and collaborate with cross-functional teams to improve data processes. Using tools like Power BI and Excel, they will generate insights and support data quality initiatives across regions.
This role involves developing and executing regulatory strategies for pharmaceutical products in the EMEA region, with a focus on oncology. The professional will support submissions to health authorities, including clinical trial applications and marketing authorization dossiers, while collaborating with cross-functional teams and regulatory agencies. Key responsibilities span pre-authorization, authorization, and post-approval lifecycle management across solid tumour therapies.
This role involves developing and executing regulatory strategies for solid tumour pharmaceutical products across Europe, the Middle East, and Africa. The professional will lead submissions to health authorities, support clinical trial applications, marketing authorizations, and lifecycle management, while collaborating with cross-functional teams and regulatory agencies. Expertise in EMA procedures and oncology regulations is central to ensuring compliance and timely product commercialization.
This role involves developing and executing regulatory strategies for solid tumour products across Europe, the Middle East, and Africa, with a focus on clinical trial applications, marketing authorisation submissions, and lifecycle management. The professional will collaborate with cross-functional teams and regulatory agencies, ensuring compliance and timely approvals for oncology pharmaceuticals. Work includes drafting submissions, responding to health authority queries, and supporting scientific advice procedures.
