4 of 4 ISO 13485 Jobs in the North of England

analysis, and corrective/preventive actions. Collaborate effectively with production, engineering, and quality teams to ensure timely resolution of quality issues. Maintain compliance with ISO 13485 and other medical device regulatory standards. Contribute to Continuous Improvement efforts in Quality/Inspection processes and documentation. Increasing efficiency, improving … ability to interpret complex technical drawings and CAD data. Skilled in using a wide range of manual measurement tools. Familiarity with ISO 13485, ISO 9001, or other regulated quality systems. Good working knowledge of Quality documentation, including FAIRs, CTQs, inspection reports, NCRs, CAPA and Complaints. Strong teamwork ...

tests Experience converting requirements into structured test cases and procedures Experience working with medical devices running embedded software Working knowledge of IEC 62304 and ISO 13485 Good understanding of the full software engineering lifecycle Able to work independently and self-manage a standalone testing function Desirable Knowledge …/or ISO 14971 Contract Details 6 month initial contract, with potential to extend 3 days per week onsite in Manchester Up to £425 per day, Outside IR35 How to Apply If you have embedded software V&V experience within a regulated medical device environment and IEC 62304/ ...

embedded/firmware literacy Hands-on engineering mindset Experience in regulated or process-heavy industries (Medical devices, aerospace, automotive, nuclear, oil & gas) Exposure to ISO frameworks (ISO 13485 is a plus but not essential) Methodical, structured, documentation-first mindset Strong communicator and growth-oriented ...

coursework deadlines Understand the Company’s obligation to quality and to apply the appropriate Standard Operating Procedures (SOPs) pertinent to the role. Comply with ISO 9001/13485 standards Understand the Company’s commitment to Health & Safety and ensure that policies, procedures and safe methods of work ...