76 to 87 of 87 ISO 13485 Jobs in the UK

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 ...

software products in a hybrid role with some remote work. The ideal candidate has a Computer Science background, embeds systems experience, and familiarity with ISO 13485, IEC 62304 and FDA requirements. #J-18808-Ljbffr ...

Nice to Have Familiarity with NHS workflows, EHR systems (EMIS, SystmOne), or care pathway design Exposure to DCB0129/DCB0160, MHRA SaMD frameworks, or ISO 13485 Familiarity with accessibility standards (WCAG 2.1 AA) in regulated or public-sector digital products Competitive salary Opportunity to work with a team ...

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 ...

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 ...

communication, interpersonal, and team-building skills. Ability to make strategic decisions, solve complex problems, and manage multiple projects simultaneously. Experience of working in an ISO 9001 or 13485 environment. Knowledge and experience with SMT machines. Working Hours Hours are 7.45am-4.30pm Monday - Thursday and 7.45am - 1pm Friday. ...

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 ...

protect margin through scoping and change control* Build efficient, repeatable delivery processes and embed AI and tooling to improve productivity* Ensure compliance with ISO 9001, 27001, 42001, 13485 and medical device regulations* Act as a senior point of contact for customers, and work closely with Sales, Product … plus confident stakeholder management and communication* A passion for coaching and developing people* Desirable: NHS/public sector delivery, clinical safety, medical device or ISO experience; PRINCE2/MSP/PMP/APM **About Us**Harris Health Alliance is part of Harris Computer, a global provider of mission-critical ...

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 ...