26 to 50 of 59 ISO 13485 Jobs in the UK excluding London

considerations and design-for-manufacture principles. Experience with electronic testing tools such as oscilloscopes, spectrum analysers, and logic analysers. Understanding of medical device standards (ISO 13485, IEC 60601, IEC 62304) is an advantage. Ability to troubleshoot and solve complex design issues. Effective communication skills for working within cross ...

bring The essentials: Degree in Electronics Engineering, Electrical Engineering, or related discipline. Proven experience in electronics design for medical or regulated devices (ISO 13485 environment preferred). Proficiency in Altium Designer for schematic capture and multi‐layer PCB layout. Strong understanding of STM32 microprocessors, BLE, power/battery … Familiarity with DFM/DFT principles and working with contract manufacturers. Understanding of wireless regulatory testing (CE/FCC) and EMC design. Knowledge of ISO 14971 risk management and medical device development processes. Embedded systems development experience. Why Neupulse? Make a tangible difference. Your work on cutting‐edge wearable ...

access management and continuous improvement. Develop, maintain and improve manufacturing software systems, electronic records, reporting tools and digital workflows in compliance with GMP, FDA, ISO 13485, 21 CFR Part 11 and applicable regulatory requirements. Lead Computer System Validation (CSV) activities, including the development and execution of Validation Plans ...

. Qualifications: Degree in Mechanical, Electrical, Mechatronics, or Automation Engineering (or equivalent hands-on experience). Pluses: Robotics integration (6-axis/SCARA), ISO 13485/GAMP knowledge, or Six Sigma training. ...

support in a pro-active manner in the form of creative solutions to problems encountered with the product. To deliver work in compliance with ISO13485 and FDA Medical Device Design Control processes. MINIMUM QUALIFICATIONS Strong academic background (2:1 Degree) in Electronic Engineering or equivalent education gained through work experience. ...

engineering (e.g., Systems, Biomedical, Mechatronics, Electronics) or related discipline. 5+ years’ experience in a regulated industry where Quality Systems are essential, e.g., ISO 13485. Expert knowledge of microcontrollers, embedded firmware development/debugging of scripts and programs. Experience of using CAD software (e.g., Altium, SolidWorks) for electromechanical designs towards ...

framework. Training and mentoring junior members of the team. Promote automation-first thinking within the testing team. Compliance with the MDD/MDR and ISO 13485/62304 standards for validation and verification of software medical devices. Skills & Experience Required: Essential Strong Python programming skills, including object-oriented ...

. Experience with software testing and verification techniques, including unit, integration, and system testing. Preferred Skills & Attributes Knowledge of medical device software standards including ISO 13485, IEC 62304, and FDA software development requirements. Experience developing software for embedded systems or hardware-integrated applications. Familiarity with safety-critical ...

electronics, you can demonstrate significant industry experience in electronic hardware design including prototyping, ECAD, test and manufacturing. Project experience with medical device regulations (ISO13485). Other highly-regulated industry experience may be considered. Experience with FPGAs or Python for test automation would be desirable. Exposure to optics, embedded software ...

electronics, you can demonstrate significant industry experience in electronic hardware design including prototyping, ECAD, test and manufacturing. Project experience with medical device regulations (ISO13485). Other highly-regulated industry experience may be considered. Experience with FPGAs or Python for test automation would be desirable. Exposure to optics, embedded software ...

critical software engineering practices Background in Computer Science and Software Development Experience in embedded systems development Knowledge of regulatory standards for medical software, including ISO 13485, IEC 62304, and FDA requirements Proficiency in programming and object-oriented programming (Python, C#, C++) Knowledge of software testing and verification techniques ...

software for medical devices or another regulated industry, such as aerospace or automotive safety Working knowledge of relevant standards and regulatory frameworks, such as ISO 13485, IEC 62304 and IEC 60601, or equivalents A strong understanding of the documentation, traceability and verification required for safety-critical software Experience ...

culture of quality through peer reviews, constructive feedback and adherence to development standards. Ensure all development activities comply with Optos' Software Development Lifecycle (SDLC), ISO 13485 and FDA Medical Device Design Control requirements. MINIMUM QUALIFICATIONS Degree in Computer Science, Software Engineering, Mathematics, or a related technical discipline ...

Docker, Kubernetes Experience with medical imaging data e.g. CT or MRI in DICOM format or clinical trial data Experience working in regulated, GxP or ISO 13485 environments Experience in respiratory or interstitial lung disease trials What can you expect from us A comprehensive benefits package that includesan annual ...

statistical acceptance criteria and data-driven testing. Biomedical, healthcare or digital-health experience. Experience in regulated medical technology environments. Familiarity with IEC 62304, ISO 13485 or related medical-device standards. We do not require previous experience specifically in hardware or embedded-software testing, web front-end testing, clinical ...

architectures, mentor engineers, and drive design for manufacturing and EMC across projects. Join a highly skilled R&D team delivering innovative solutions while ensuring ISO13485 and FDA design control compliance. Excellent problem-solving and cross-functional collaboration are essential. #J-18808-Ljbffr ...

site. Liaison with Fitters and Test Engineers. Building prototype assemblies. Meet appropriate company, national and international standards in product design, e.g., ISO61010, ISO13485, 21CFR820 etc. To keep up to date with available third-party components. To keep up to date with design techniques of analogue and digital circuits as well ...

collaborate across engineering teams to deliver reliable diagnostics. The role requires an MSc in engineering and 5+ years in a regulated environment with ISO 13485, strong firmware and CAD expertise (Altium, SolidWorks) and robust problem-solving. #J-18808-Ljbffr ...

service for assistive technology users. You’ll coach and develop technical staff, diagnose faults, collaborate with Hardware Engineering to improve product reliability, and drive ISO 13485 readiness and regulatory compliance across the #J-18808-Ljbffr ...

device experience advantageous Project management experience beneficial High-speed PCB design Embedded systems and firmware development Desired PLCs EMC, LVD and RED IVDR/ISO 13485 Machinery Directive experience Company Information My client is a market-leading manufacturer continuing to invest in new product development and growth. They ...

device experience advantageous Project management experience beneficial High-speed PCB design Embedded systems and firmware development Desired PLCs EMC, LVD and RED IVDR/ISO 13485 Machinery Directive experience Company Information My client is a market-leading manufacturer continuing to invest in new product development and growth. They ...

ability to assess and improve working practices within the Warehouse. Competence in Vitalograph procedures and the Quality Management System (QMS). An understanding of ISO 13485, the Medical Devices Directive and GCP, as required. If youre looking for a hands-on role where you can develop your technical ...

frequent travel. Desirable (nice to have): Experience in magnetic shielding, sensing, or low noise environments. Background in biomedical device installation, especially neuroimaging. Familiarity with ISO documentation practices and standards (e.g., ISO 9001, 13485). What you will bring to Cerca: Precision and reliability—ensuring every system performs ...

speed, and extend coverage across tests for medical device software validations. You will mentor juniors and promote automation-first practices while aligning with ISO 13485/62304 compliance requirements. #J-18808-Ljbffr ...

Strong understanding of software development lifecycle and version control (e.g., Git). Desirable experiences for an Embedded Software Engineer: + Experience with IEC 62304, ISO 13485, or FDA 21 CFR Part 820 + 3+ years of experience in a regulated industry Apply today to join a highly innovative ...