/Medical Device Quality Assurance department. - Knowledge of GxP and Quality related regulations and standards within the Pharmaceutical/Medical Device industry. - Familiarity with ISO9001, ISO 13485, GCP is essential. - Knowledge of ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor would be more »
continuous development software life cycle models Version Control Experience of Electronic hardware An understanding of control system elements (sensors, actuators, controllers) would be useful. ISO9001: 2015 lead auditor CML Offers: We have roles that you can help define and mould your skills and ambitions within a multi more »
scalable, allowing personalised therapies to be affordable for more people. To commercialise their technologies, they are recruiting a Quality Manager to lead them through ISO9001 and other regulations. This would include developing and building quality frameworks for all stages of project development and manufacture through the management … in from all stakeholders. Requirements: Graduated with a bachelor's or master's in engineering or similar. Substantial demonstrable experience leading a company through ISO9001/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality … considered. On offer is a healthy benefits package including private medical insurance (including immediate family dependents), enhanced company pension contributions and annual bonus. Keywords: ISO9001/13485, Quality Management, Auditing, Medical Devices, Regulations, Development, Manufacture, Cambs/Herts Border Another top job from ECM, the high-tech recruitment experts. Even more »
Essentials: - - Degree level or above in electronics or similar discipline. - Significant experience of working within a high-volume electronics manufacturing environment - Auditing experience to ISO9001 standards. (Ideally a lead auditor) - working knowledge of 8D and continuous Improvement You will be working or ground breaking technology, offered a more »
8D problem solving methodology. You will also play a key role in the internal auditing process, ensuring the business stays on-track for its ISO9001 certification. The technology under development represents a close coupling of mechanical, electrical, control, and software systems and alterations to any one area … and electro-mechanical hardware testing. Requirements: Commercial experience as a quality engineer or similar at a high-volume electronics manufacturing company Strong familiarity with ISO9001 Good degree (1st or 2:1) in an engineering discipline Full and unrestricted rights to work in the UK Based in Cambridge … expand and strengthen their skills, learning from expert colleagues from a variety of technical backgrounds. An excellent salary is on offer. Keywords: Quality, QMS, ISO, ISO:9001, 8D, PDCA, Continuous Improvement, Lead Auditor Another top job from ECM, the high-tech recruitment experts. Even if this job more »
Cambridge, Cambridgeshire, East Anglia, United Kingdom
Bluegate Consulting Ltd
/HNC level or above in electronics or similar discipline. - Significant experience of working within a high-volume electronics manufacturing environment - Auditing experience to ISO9001 standards. (Ideally a lead auditor) - working knowledge of 8D and continuous Improvement You will be working or ground breaking technology, offered a more »
considered for the Principal Test Engineer vacancy you must have: Prior experience in a related position/field Knowledge of quality systems such as ISO9001:2015 Experience with both LabVIEW and Python Experience with complex electronics testing An understanding of sensor technology (ideally MEMS/gas sensors) If you have more »