Future Tech Jobs
Future Tech Jobs
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.
This role involves delivering high-level technical training and support for the Medtronic Hugo RAS robot, covering surgical indications in General Surgery, Urology, and Gynaecology. You will train surgeons, first assistants, and OR staff, apply structured teaching methodologies, and collaborate with sales and clinical teams to prepare and set expectations for training programs.
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are looking for a Contract Excellence Lead for our International region to join our Commercial Centre of Excellence. In this influential role, you will shape...
Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.We are looking for a Contract Excellence Lead for our International region to join our Commercial Centre of Excellence. In this influential role, you will shape...
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 Clinical Trial Leader will support the planning and execution of clinical trials for medical devices, working closely with cross-functional teams, clinical sites, and external partners. The role involves ensuring quality and compliance while contributing to innovative medical device development that improves patient outcomes.
Act as the technical authority for legislative compliance and product safety in medical equipment, conducting rigorous testing, maintaining certification records, and contributing to product design for compliance. Lead audits and training to ensure adherence to ISO and MDR standards within a collaborative, innovation-driven environment focused on accessibility solutions.
This role involves driving the development of next-generation surgical and interventional devices using advanced ultrasound technology. Responsibilities include leading high-impact technical programmes, collaborating with partner organisations, and applying scientific expertise from feasibility studies to market preparation.
This role involves ensuring quality assurance and regulatory compliance across the full lifecycle of advanced medical devices, from design through manufacturing, for global markets including Europe, North America, and APAC. The specialist will conduct internal audits, help shape regulatory strategy, and work with complex, innovative technologies in a high-autonomy environment. The role focuses on new product development, requiring strict adherence to ISO 13485, CE Marking, and other international standards.
This role involves providing expert clinical and technical support during electrophysiology procedures in hospitals, delivering training on advanced medical devices, and collaborating with sales teams to promote EP technologies. The associate will receive comprehensive training and work closely with clinical professionals, supporting product use and staying current with evolving cardiac therapies. Frequent travel across a defined territory is required, with a focus on hands-on technical and educational support in real-world medical settings.
The Scientist role involves reviewing clinical data, writing technical reports, and ensuring medical devices meet regulatory requirements for CE marking and global approval. You will collaborate with a scientific and clinical team, prepare high-quality reports, and manage changing priorities in a fast-paced environment.
This role involves daily repair, preventative maintenance, and asset management of medical devices across multiple hospital locations. Key responsibilities include performing scheduled maintenance, completing repairs, and ensuring minimal disruption to hospital operations. The role requires strong customer support skills and the ability to maintain safe working practices in a healthcare environment.
This role involves leading the product development lifecycle for complex medical technology products, from concept to launch and ongoing support. Responsibilities include managing R&D projects, providing strategic direction, mentoring a specialist team, and collaborating with various departments to ensure product success and regulatory compliance.
Leads end-to-end engineering and product development for complex electromechanical medical devices within a regulated environment. Responsible for overseeing R&D, NPI, and a critical in-flight next-generation product programme, ensuring compliance with ISO 13485 and UK/EU MDR standards. Works cross-functionally with quality, regulatory, manufacturing, and commercial teams to deliver innovative, compliant products from concept through to production and support.
This role involves supporting the Quality Management System (QMS) and Regulatory processes, including ISO13485 readiness and FDA 510(k) documentation. You will work closely with internal teams to maintain quality documentation, manage change controls, and promote continuous improvement.
