1 to 3 of 3 Quality Management Jobs in Cambridgeshire with Remote Work Options

Reporting to the Group Quality Manager (who is also our Group Data Protection Officer), the Regulatory & Quality Engineer ensures that the company's quality policy is implemented and respected, and plays a pivotal role in matters relating to the Quality Management System. Operating in an … ordinate customer audits , including scheduling, preparation, execution, and follow-up activities. Conduct regular internal audits to identify areas for improvement and ensure adherence to quality standards. Manage the process of responding to customer questionnaires and feedback, ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting … supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators (KPIs) and metrics to measure and monitor quality performance throughout more »

Degree or equivalent. Knowledge of MAX MRP System, Defence Standards and Environments. Awareness of military support solutions, skills and capabilities. A strong understanding of Quality Management and Control systems. Knowledge and use of ILS, Supportability and R&M techniques (including Windchill-RELEX software). Knowledge of Health, Safety more »

to become more cost-effective and scalable, allowing personalised therapies to be affordable for more people. To commercialise their technologies, they are recruiting a Quality Manager to lead them through ISO 9001 and other regulations. This would include developing and building quality frameworks for all stages of project … development and manufacture through the management of a digital document quality management system (QMS). This will require good communication skills to get buy-in from all stakeholders. Requirements: Graduated with a bachelor's or master's in engineering or similar. Substantial demonstrable experience leading a company …/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality management" within a technology company including instilling a quality-focused culture and maintainable approach to quality processes. Detail oriented and strong more »