51 to 70 of 70 ISO 13485 Jobs in England

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 ...

other safety-critical systems . Experience within regulated environments or lifesciences would be an advantage. Being Highly proficient with AI. Knowledge of IEC 62304 , ISO 13485 or similar regulated software development standards. Experience with medical alarm systems or other alarm and fault-management systems. Understanding ...

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 ...

regulated environment. Familiarity with document management or OCR tools. Experience using Jira and Confluence. Awareness of clinical governance or quality frameworks (for example GxP, ISO 13485, DCB0129/0160). What success looks like in the first 6 months Full ownership of e-sign configuration and first-line ...

mission-critical or highly regulated software . Desirable Skills & Experience Experience developing medical devices or other safety-critical systems . Knowledge of IEC 62304 , ISO 13485 or similar regulated software development standards. Experience with medical alarm systems or other alarm and fault-management systems. Understanding ...

safety-critical, mission-critical or highly regulated software. Desirable Skills & Experience Experience developing medical devices or other safety-critical systems. Knowledge of IEC 62304, ISO 13485 or similar regulated software development standards. Experience with medical alarm systems or other alarm and fault-management systems. Understanding ...

hardware design, prototyping and ECAD work in a collaborative MedTech setting. Using Altium Designer, you will prototype, test and optimise architectures while complying with ISO13485 and related standards. Some travel may be required for international customer and supplier interactions. #J-18808-Ljbffr ...

defining the vision. Nice to have: experience in medical devices or another regulated hardware/software environment, with exposure to documentation practices under ISO 13485 or IEC 62304. Nice to have: prior experience setting up or overhauling a ticket intake and triage process from scratch, rather than inheriting ...

other cancers a plus) International experience (work or study abroad) esp in North America, Europe and APAC Experience working within regulated environments (e.g. ISO 13485) What we offer Work that is both challenging and rewarding and has a real positive impact on people's lives Fast growth, ownership ...

Engineer to join their innovative medical devices team. The role involves developing safety-critical embedded firmware for insulin pump systems while ensuring compliance with ISO 13485 and other relevant standards. You will lead firmware architecture and work closely with cross-functional teams to establish best practices. The ideal ...

organise complex programs of work as part of a team, but often working alone in isolated environments. To work in accordance with the departmental ISO 9001 quality system. Ensure all servicing tools and test equipment are functional and organise repair and maintenance as required. To participate as required … patient-facing clinical environment. Experience of scheduled maintenance programmes and in meeting targets. Experience of working within a Quality Management System such as ISO 9001 and ISO 13485. Experience of delivering teaching and training to technical staff Desirable Experience of delivering teaching and training to clinical staff. Skills ...

users. GxP-aware delivery. Deliver all technical support activities to a high standard, in line with Qureight SOPs and relevant regulations, including GxP requirements, ISO 27001 standards and data privacy regulations. To thrive in this role, you'll need: Previous experience in a technical support, application support, IT support … Zendesk or JIRA. Knowledge of Good Clinical Practice (GCP) with evidence of recent training. Experience working within a Quality Management System (QMS), e.g. ISO 9001, ISO 13485. Knowledge of relevant clinical trial regulatory, compliance and industry standards. Track record of working effectively and problem solving in a highly ...

Reset Health are looking for an experienced Scrum Master to serve and guide two agile development teams in our engineering group. Our Live Platforms team is our development ‘fast lane’ making production releases at the ...

role requires a keen user-centric mindset and ability to work with people across the business. You’d be responsible for: Knowing the ISO standards applicable to us (13485, 14971, 62304, 82304 in particular) and understanding how they map onto day-to-day Flok activities and tools Helping ...