76 to 100 of 222 QMS Jobs in England

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 development. Requirements: Bachelor's degree more »

Auditing and measurement of CCP - Testing of equipment - Sample collection - Conducting hygiene audits and reporting findings to arrange any corrective action - Update the Quality Management System - Assessment of raw materials and finished products against relevant specifications Experience: - Previous experience in a quality assurance role, preferably in a manufacturing or food more »

/FDA regulated environment. Implement verification and validation test plans and protocols for the system/product, documenting all activities within the Quality Management System (eQMS). Collaborate with the Engineering and quality departments to ensure test method, equipment and materials are available in line with company timelines. Analyse and more »

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 Biology teams working more »

and validation processes to prepare the system for clinical studies and FDA approval. Implement test plans and protocols, documenting all activities within the Quality Management System (eQMS). Develop Work Instructions and Standard Operating Procedures (SOPs). Collaborate with Engineering, Manufacturing, and Biology teams to achieve regulatory submission and product more »

Testing, fault finding and repair of electronics. Completion of test reports and documentation in accordance with customer requirements and in line with the Quality Management System standards. Upgrading and modification of assemblies and finished product. Interpretation and implementation of changes to assemblies and finished product in accordance with documentation. Identifying more »

team Facilitate project progress meetings with the project team Lead communications with suppliers and clients Contribute to sales activities, marketing materials and the Quality Management System as required What skills and knowledge can I bring? Experience managing the development of firmware for embedded products and systems (user interfaces, sensors, wireless more »

Professional Engineering Qualifications * Good knowledge and experience of engineering manufacturing processes/techniques, especially, stamping and injection moulding. * Good knowledge and experience of Quality Management System requirements. Further details: * Monday - Thursday 8:00am to 5:00pm & Fridays 8am to 1pm. * On site * Based in Portsmouth Refer a friend and earn more »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

and processes regularly. Maintain and align HACCP (HACCP/TACCPVACCP) program is maintained and aligned with best practice at all times Implement and amend QMS for product standards. Ensure effective QA and Hygiene team management. Implement pest control mechanisms for food safety. Conduct trend analysis of quality issues. Manage internal more »

milestone progress to the Project Lead, Programme Manager and Stakeholders. Maintain best practices within the Software Team, ensuring technical journals, essential research and company QMS process are followed. Leadership and administration of the Sprint process for the Software Team. Support the delivery of product firmware and software within the Software more »

and Qualifications: Demonstrated experience in the design and development of products - Medical industry advantageous Design or Engineering Degree preferred Familiarity with regulatory standards and QMS - ISO13485 advantageous CAD proficient, preferably Solidworks Plastic manufacturing process knowledge If you want to be part of a team dedicated to making a meaningful impact more »

ready to step up into a Principal role or an established PA looking for a change in their career. The Role: Adherence to the QMS including root cause analysis and communicating with clients on technical matters. Assistance in maintenance programs for the Departments specific analytical instrumentation and any other analytical more »

devices and systems, including design for quality activities and working to develop a capable and robust/stable process. Adhere to Quality Management System (QMS) requirements in line with Corin’s ISO13485 QMS & Good Manufacturing Practice (GMP) FDA21 CFR Part 820. Support brainstorming and problem-solving as required activities for more »

of KPIs Deputise for the QARA Manager & RP where appropriate Support the QA/RA Manager & RP in ensuring that a quality management system (QMS) is implemented and maintained including quality risk management, documentation management, non-conformance and CAPA, change management, deviation processes, internal and supplier approval and audits as … of operations/sales staff & QA peers Generation, issue and archive of non-project and project-controlled documentation Create all metrics associated with the QMS and report these to the QA/RA Manager, also feed these into the BMR and monthly reports. Proactive generation and timely review/implementation … of the requirements of the MDD/MDR as well as ISO13485 & ISO9001 Ability to work in matrix teams. Experience of working with multiple QMS systems Understanding of the requirements of GDPR & ISO27001 Basic knowledge of the principles of Lean six sigma and its application Relevant Science or Engineering based more »

join the company. Permanent role with a competitive starting salary and extensive benefits package. Job Overview: Maintenance and improvement of the Quality Management System (QMS). Assure the compliance of all activities with Good Distribution Practice (GDP) and Good Manufacturing practice (GMP) requirements. Responding to medical information enquiries from healthcare more »

Energy Business Management System Quality Requirements PROJECT RELATED: Understand and Interpret Client’s Quality Requirements to ensure compliance. Developing and Maintain a project quality management system and ensure implementation Develop Project Quality Plan, Inspection & Test Plan & and required project quality procedures. Support the overall Project QAQC Team. Assist in monitoring more »

Monitoring) for Part21J knowledge with aviation regulations, including CAA EASA, FAA. line leader for a team of Quality professionals across multiple locations. the companies QMS and quality systems. continuous improvement of Quality business systems. portfolio of external and customer Quality approvals. and conduct internal audit plans covering approvals and certification. more »

Manufacturing support to the production areas with reference to quality issues Ensuring procedures are implemented or updated where appropriate. Actively support the business with QMS to ISO 9001:2015 certification Key skills and experience for the Quality Engineer job are: Previous work experience as a Quality Engineer or similar role more »

formal qualification in quality, although this isnt essential. About the Job Youll take the responsibility of ensuring products are manufactured meet the customer specifications. QMS maintenance that complies with ISO9001. Youll lead a small team, youll be able to influence and motivate to ensure goals are met. Youll ensure internal more »

in upholding the highest standards of quality! For this role,you must be willing to obtain CTC clearance Key Duties • Active promotion of Quality Management system awareness. • Review and update site quality plan • Produce and review Inspection and Test Plans and monitor compliance • Production of Work Packs • Weld Inspection (only more »

Manufacturing and/or Engineering, looking to significantly progress their career with continued training and career support, alongside generous company benefits. The Role: Ensure QMS compliance Drive quality and process improvement Generate documentation and supplier assessments Support Quality Control where needed The Person: Quality Engineer and/or similar Background more »

conformances and collaborate on CAPA objectives. Working with the Leadership Teams as well as building positive and effective relationships with other internal stakeholders on QMS related activities. Ready to apply? This is what you will need to demonstrate; Qualified/Certified Auditor for ISO 13485 (please note, this is a more »

post holder will assist the senior laboratory BMS in the delivery of a high quality, efficient and effective service, through the Quality Management System [QMS]. They will assist in the implementation of change as directed by the laboratory seniors/manager, when delegated or appropriate to service needs. The … post holder will assist the senior laboratory BMS in the delivery of a high quality, efficient and effective service, through the Quality Management System [QMS]. They will assist in the implementation of change as directed by the laboratory seniors/manager, when delegated or appropriate to service needs. The more »

team, work under pressure and meet deadlines. Main duties of the job You will enjoy a varied range of responsibilities from maintaining the quality management system and UKAS accreditation, training and supervision of less experienced members of staff, validating and authorising results and most importantly providing a safe quality service more »