Future Tech Jobs
Future Tech Jobs
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.
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...
The Mechanical Design Engineer, Consumables role involves hands-on design, development, and verification of next-generation class III consumable perfusion sets. You will work within a cross-functional R&D team, collaborating with internal and external stakeholders to ensure high-quality product delivery and compliance with regulatory standards.
The Electronics Design Engineer will design, develop, and support electronics systems for OrganOx’s medical devices, ensuring compliance with regulatory and safety standards. Responsibilities include full lifecycle electronics design, from concept to manufacturing, with a focus on reliability, safety, and manufacturability.
As an R&D Engineer, you will work within a collaborative team to develop the next generation of medical devices, from early concept to clinical trials and manufacturing. Your role involves planning and delivering engineering work packages, translating user needs into engineering requirements, and working closely with cross-functional teams to ensure robust design outputs and regulatory compliance.
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 role involves performing the legal duties of a Qualified Person (QP) for the manufacture and certification of investigational medicinal products, ensuring compliance with EU regulations and GMP standards. Responsibilities include batch certification, quality management, and ensuring the effectiveness of pharmaceutical quality control systems.
The Business Analyst will support a key programme focused on the collection, tracking, and lifecycle management of human biological samples. Responsibilities include eliciting and documenting requirements, mapping end-to-end processes, and facilitating workshops with scientific and technical teams to enhance biobanking systems and data flows.
Want a 3D Career? Join Norgine.At Norgine, our colleaguesDare themselves to be different and try new things,Drive to achieve their goals and beyond, andDevelop themselves and their community.We call it the3D career at Norgine and it offers you a fully-rounded...
The Project Manager will manage complex medical device tooling and injection moulding projects from customer handover to production release. Key responsibilities include coordinating cross-functional teams, maintaining project plans, and ensuring compliance with ISO 13485 standards.
The Founding QMS Architect will build a lean, scalable Quality Management System for a fast-paced, advanced manufacturing company. This role involves creating compliance frameworks, driving certification strategies, and coordinating with external regulatory experts to support rapid product delivery across regulated industries like aerospace, defence, and medical devices.
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.
Cure Talent are delighted to be partnered with a global manufacturer of medical technology, part of a wider FTSE 100 group, supporting healthcare professionals worldwide with innovative instrumentation.We are looking for a Quality professional to join the team in a...
This role involves developing and implementing embedded firmware solutions, designing and integrating electronic hardware, and working closely with cross-functional teams to bring next-generation scientific instruments to market. You will be part of a multidisciplinary R&D team, contributing to the entire product lifecycle from concept to production.
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.
