1 to 7 of 7 Quality Management Jobs in Cambridge

the short application form on our website. We’re interested in hearing from candidates with experience in the following areas: Key Account and Product Management Quality Management Mechanical Engineering Mechanical Design Electronics Engineering Mechatronics Engineering Software Engineering (industrial automation, embedded) Verification and Validation Engineering Cellular Origins Cellular more »

Hobson Prior is seeking a Quality Assurance Specialist on a permanent basis. This role focuses on maintaining and improving the Quality Management System (QMS) whilst developing diagnostic capabilities. This includes supporting internal audits, assisting with client audits, and providing support for quality department initiatives. Responsibilities: - Work … all aspects of the QMS, including Change Controls, Non-Conformities, CAPAs, and Customer Complaints. - Support continuous improvements in the QMS and maintain compliance of Quality processes by conducting internal audits. - Assist with audits, both internally and externally, including desk-based, remote, and on-site audits of subcontractors and suppliers. … Work with other Quality Assurance staff to provide support to departments, such as reporting on Quality Metrics and assisting in training personnel on matters relating to the QMS. - Support Quality department initiatives as part of a multi-disciplinary team. Key Skills and Requirements: - Experience working within a more »

Validation Engineer who will actively engage in hands-on testing of the LEX diagnostic system. You will be working closely with the head of Quality and Engineering team and will be responsible for defining, designing, and executing verification and validation activities for the LEX 5-minute PCR diagnostic platform. … for clinical study and FDA approval. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Contribute to the development of Work Instructions and Standard Operating Procedures (SOPs). Collaborate with the Engineering, Manufacturing and … forefront of point-of-care diagnostics for over 20 years. Drawing upon the expertise of its consultants in the Life Science sector, and the management experience of a company with a 30-year track record of developing breakthrough technology and creating ambitious tech businesses, TTP Group invested core IP more »

upcoming product lines. Your duties will involve testing a diverse range of devices, creating effective test methods and fixtures, and ensuring strict adherence to quality standards. Key Responsibilities: Contribute to the V&V process for new product development, including testing various devices and designing appropriate test methods and fixtures. … protocols, document procedures, and prepare comprehensive reports in accordance with design control standards. Background in the medical device sector to understand regulatory requirements and quality management systems (QMS) essential for successful product development. (ISO13485) Knowledge in mechanical engineering with a focus on testing equipment and innovation in product … in Electronics or Mechanical Engineering. Up to 5 years of proven experience in testing equipment and product development. Strong understanding of regulatory requirements and quality management systems in the medical device sector. If you are having difficulty in applying or if you have any questions, please contact Jaeme more »

is to ensure the NHS in England has a sufficient and inclusive workforce with the knowledge, skills, values, and behaviours to deliver compassionate high-quality health and care to the people it serves. The WTE directorate delivers multi-professional education and training, and proactively engages with systems and partners … priority and with a geographical remit. Lead the delivery of the East of England regional programme and regional oversight of the national programme, including quality management processes. Actively manage and support Training Programme Facilitator and Education Supervisors through leadership and facilitation of networks, in all sectors and leading … new NHS England board have set out the top-level purpose for the new organisation to lead the NHS in England to deliver high-quality services for all, which will inform the detailed design work and we will achieve this purpose by: Enabling local systems and providers to improve more »

Job summary Are you highly motivated with a positive attitude to change, a proven record of resource management, team building and excellent leadership qualities? Cambridge Genomics Laboratory, Lead Laboratory of the East Genomic Laboratory Hub is inviting applications for a Consultant Clinical Scientist to lead the cancer service in … Genomic testing to be at the forefront of diagnostic capability and national change. You will become an integral part of the laboratory's senior management team and work closely with the wider East Genomic Laboratory Hub leadership team to ensure successful delivery of the cancer service as part of … deputy head for the Cambridge Genomics Laboratory being responsible and accountable for the delivery of the overall genomic healthcare service Provide overall direction and management of a comprehensive efficient and high quality genomics service for patients Provide leadership and expert consultative management advice for the entire genomics 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 »