51 to 59 of 59 ISO 13485 Jobs in the UK excluding London

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 ...

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 ...

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. ...