Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
This role involves driving sales and market share for Transcatheter Aortic Valves (TAVI) and Transcatheter Pulmonic Valves (TPV) in the Midlands. Responsibilities include developing therapy plans, engaging key stakeholders, and providing technical support and training to hospital staff.
The Regulatory Affairs Manager for the UK and Ireland leads the QRA team, ensuring regulatory compliance, post-market surveillance, and quality system adherence to ISO 13485. They act as the primary contact with UK and Irish regulatory agencies, manage import licences, and coordinate audits and inspections.
As a Regulatory Affairs Specialist, you will work across regions and products, preparing global regulatory submissions and maintaining compliance for Smith & Nephew's orthopaedic portfolio. You will collaborate with project teams to develop regulatory strategies, support product changes, and ensure adherence to international regulations.
The Staff Systems Verification Engineer will lead the development and execution of test strategies for digital and electromechanical medical devices, ensuring compliance with regulatory standards. They will work closely with cross-functional teams to create and maintain test environments, including automation, and improve team productivity.
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.
This role involves assembling high-quality medical devices within a controlled cleanroom environment, ensuring products meet strict quality and compliance standards. Responsibilities include precision component assembly, labelling, and packing, while working efficiently in a fast-paced, high-volume production setting.
The Patient Safety Partner will support individual case safety reports, assess pharmacovigilance requirements, and manage local safety risks within ophthalmology. They will also assist with global safety solutions, product launches, and cross-functional team collaboration, contributing to audits and continuous improvement activities.
This role involves servicing and repairing sophisticated medical and laboratory diagnostic systems used in pathology departments and NHS laboratories. You will visit customer sites, troubleshoot issues, and liaise with laboratory managers and technicians. Full product training is provided, and the company is a global leader in medical and laboratory equipment.
The Chief Technology Officer will lead the technology and product development strategy for a rapidly growing MedTech company. Key responsibilities include guiding multidisciplinary teams, translating customer and commercial requirements into product priorities, and ensuring regulatory compliance. The role involves close collaboration with executive leadership and external stakeholders.
The Senior Project Manager will lead complex projects across the Specialty Diagnostics Group, focusing on business transformation and change control. Key responsibilities include managing project tasks, budgets, risks, and documentation, as well as mentoring staff and contributing to strategic direction.
The Senior Pharmacovigilance Scientist will lead safety signal management activities, including detection, evaluation, and assessment of safety signals. They will also oversee aggregate reports, respond to safety queries, and ensure compliance with global safety regulations and guidelines.
This hands-on role involves assembling, servicing, and repairing precision medical devices such as Automatic Dose Dispensers (ADDs). You will handle small mechanical and electrical components, follow technical drawings, and support stock management. The role offers significant career progression within a rapidly growing business.
This role involves assembling high-quality medical devices in a cleanroom environment, following strict GMP standards and ISO procedures. The position offers a 4-day work week, with opportunities for overtime and a range of benefits including private healthcare and a company pension.
The Technical Moulding Manager will lead and optimize injection moulding processes in a regulated ISO 13485 environment, ensuring process validation, continuous improvement, and technical support. Key responsibilities include process ownership, technician leadership, and collaboration with NPI, Tooling, Quality, and Operations teams.
The Global Clinical Study Manager will oversee the end-to-end delivery of complex clinical studies, ensuring milestones, timelines, and budgets are met. Key responsibilities include managing cross-functional teams, coordinating with vendors, and ensuring compliance with regulatory requirements. This role requires strong leadership and project management skills, with a focus on driving high-quality study execution in a fast-paced environment.
