This role involves providing intraoperative clinical support for cranial and spinal procedures, managing inventory, and delivering clinical and technical education programs. The position requires regular travel within the South West of England and strong collaboration with healthcare professionals and commercial teams.
The Senior Market Development Manager will drive the adoption and growth of innovative cardiac therapies like Aurora EV-ICD™, OmniaSecure™, and CSP across the UK and Ireland. Key responsibilities include developing market strategies, optimizing patient referral pathways, and collaborating with healthcare stakeholders to support service development and pathway transformation.
This role involves supporting complex orthopaedic revision surgeries by acting as a trusted advisor to surgeons and key accounts, with a focus on driving adoption of innovative technologies including robotics. The specialist will operate in the M1 corridor and East of England, developing account strategies, supporting tenders, and launching new products. The position requires extensive travel and independent management of high-volume surgical centres.
Serve as a clinical and sales expert for orthopaedic revision products, supporting surgeons in complex procedures and driving adoption of innovative technologies including robotics. Develop strategic account plans, acquire new customers in high-volume centres, and contribute to tenders and product launches. Operate with significant autonomy while collaborating with commercial teams to expand market presence in the East of England.
This student placement role involves maintaining and updating clinical evidence resources, reviewing scientific literature, and creating scientific communications and training materials. The role offers exposure to various departments and projects, including national and international scientific initiatives, and provides opportunities to participate in STEM outreach events.
This 12-month industrial placement offers hands-on experience in medical device development, including designing implants, surgical instruments, and test methodologies. You'll work with advanced technologies like robotics and 3D printing, collaborate with multi-functional teams, and contribute to product validation and regulatory documentation.
This role involves servicing, installing, and repairing sophisticated medical laboratory automation systems across Europe. You will work with a variety of scientific products in pathology departments, research labs, and pharmaceutical environments, requiring extensive travel and overnight stays.
This role involves servicing, installing, repairing, and calibrating sophisticated medical laboratory automation systems across Europe. You will support scientific products in various settings, including pathology departments, university research labs, and pharmaceutical environments, with extensive travel and frequent overnight stays.
This role involves driving software safety activities for medical devices, conducting hazard analysis and risk assessments, and ensuring compliance with medical device standards. You will collaborate with cross-functional teams and support verification and validation processes.
The Calibration Engineer will calibrate and verify the performance of ProSim medical simulators at a client’s facility, ensuring accuracy, reliability, and compliance with ISO standards. They will work closely with the client’s laboratory, engineering, and quality teams, maintaining detailed records and addressing non-conformances.
As a Production Operative, you will work in a methodical and organised manner to assemble medical devices according to design specifications and engineering drawings. Responsibilities include checking components, completing documentation, and ensuring quality and safety standards are met.
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.
This role involves developing new business and building a strong sales pipeline for medical equipment in the Midlands and North Wales. You'll work with NHS and private hospitals, delivering product demonstrations and managing complex procurement processes.
This role involves managing and growing sales in a well-established territory covering South West England and Wales. Responsibilities include developing new business, maintaining existing accounts, and engaging with various healthcare stakeholders through product demonstrations and complex sales processes.
The Regulatory Affairs Manager will lead day-to-day regulatory activities, maintaining and developing technical documentation for existing and future medical devices and IVD products. You will support UKCA and CE marking, contribute to regulatory strategies, and collaborate with scientific, data, and technical teams to ensure compliance throughout product development.
