As a Senior Platform Engineer in Medtronic's AI and Data Science Platform team, you will design, build, and maintain cloud and on-prem infrastructure to support ML Engineers, Data Scientists, and new product development. You will collaborate across teams to improve reliability, usability, and developer experience, using cutting-edge technologies like Kubernetes, AWS, and Terraform.
As a Senior Software Engineer, you will develop high-performance video and AI processing pipelines for use in the operating room. You will work closely with multidisciplinary teams to create robust and safe-by-design software, leveraging hardware acceleration and real-time video manipulation.
The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal clinical outcomes by providing expert-level support, analyzing sub-optimal results, and collaborating with various stakeholders to improve product performance and patient care.
The Medical Affairs Specialist supports the use of Intraocular Lenses (IOLs) through proctoring, case analysis, and managing Medical Information Requests (MIRs). They ensure optimal clinical outcomes by providing expert-level support to healthcare professionals and collaborating with various teams to analyze and improve patient outcomes.
Perform microbiological testing on raw materials, environmental samples, and finished products to ensure product safety and regulatory compliance. Support QA investigations, data trending, and continuous improvement initiatives in a GMP-regulated laboratory environment. Collaborate with cross-functional teams to maintain high-quality standards in manufacturing operations.
This role involves managing regulatory compliance for advanced wound care medical devices throughout their lifecycle, including preparing global regulatory submissions, guiding product development teams, and liaising with regulatory authorities. The specialist ensures adherence to standards such as ISO 13485, FDA 21 CFR Part 820, cGMP, and cGDP, while reviewing product documentation and supporting continuous improvement. Based in Hull, the position operates within a collaborative, global team environment focused on bringing innovative healthcare products to market.
This role involves providing regulatory expertise for in vitro diagnostic (IVD) and medical device innovation projects, from concept to commercialisation. The specialist will support global regulatory strategies, ensure compliance with standards like IVDR and MDR, and collaborate with cross-functional teams. The position also includes assessing emerging regulations and supporting submissions to notified bodies and regulatory authorities.
This role involves programming, setting up, and operating fibre and diode laser marking systems to mark orthopaedic implants and medical devices, ensuring precision and compliance with customer specifications. The technician will also carry out final finishing processes including cleaning, passivation, and visual inspection in a clean, quality-focused manufacturing environment. The position supports production traceability and continuous improvement while working collaboratively within a skilled team.
Operate packing processes in a regulated medical manufacturing environment, following SOPs, GDP, and GMP standards. Responsibilities include batch documentation, equipment fault reporting, quality communication, and maintaining a clean, compliant workspace. Work collaboratively with QA and adhere to health and safety protocols in a stable, long-term temporary role.
Lead a maintenance team responsible for ensuring the reliability and compliance of laboratory, manufacturing, and facility assets in a regulated environment. Coordinate planned and reactive maintenance, oversee contractor activities, and support continuous improvement initiatives. The role combines technical leadership with hands-on oversight across critical systems including GMP facilities, cleanrooms, and utilities.
The Transport Operator ensures smooth daily transport operations by managing delivery scanning, manifesting, and tracking in compliance with SOPs and regulations. You'll support drivers through briefing and debriefing using transport management systems, resolve delivery issues, maintain customer communication, and uphold health and safety and DVSA compliance standards. The role involves administrative coordination, incident reporting, and cross-dock activity within a pharmaceutical logistics environment.
Recruitment Consultant (Tech and Engineering)Bristol City Centre£35,000 basic 40% Commision + 25 Days Holiday + Rapid Progression + Personal DevelopmentAre you looking for a lucrative career in the world of recruitment, where you will be paired with a Senior Manager...
This role involves developing and delivering national sales strategies for healthcare equipment, specifically in the Moving & Handling sector. You will lead new business development, expand existing accounts, and collaborate with the sales team to achieve revenue and margin targets.
Adexa Labz provides point-of-care diagnostic solutions that enable healthcare professionals to obtain accurate blood test results in as little as 3–15 minutes, helping them make faster, better-informed clinical decisions without the delays associated with conventional laboratory testing.For care and nursing...
This role involves maintaining and servicing laboratory, cleanroom, and production equipment in a regulated environment. Responsibilities include fault-finding, implementing corrective actions, and ensuring compliance with ISO 13485 standards. The position offers opportunities for continuous improvement and collaboration with R&D and Quality teams.
