51 to 75 of 215 Permanent QMS Jobs in England

errors and reduce overall cost of Quality Monitor output, quality & scrap rates. Improving OTD performance Maintain records of products and approved suppliers Continually improve QMS processes If you are interested in this position, please apply with an up to date CV as soon as possible, along with your availability and more »

Undertake, articulate the benefits of, and assist the development of a variety of assurance and improvement activities, including audit. Develop and maintain a quality management system and controls to meet the requirements of ISO17025 and Def-Stan 05-055. Collaborate across multi-functional teams, advocating for quality throughout all more »

Undertake, articulate the benefits of, and assist the development of a variety of assurance and improvement activities, including audit. Develop and maintain a quality management system and controls to meet the requirements of ISO17025 and Def-Stan 05-055. Collaborate across multi-functional teams, advocating for quality throughout all more »

the administrative aspect of the Technical Department taking responsibility for the day to day management and maintenance of some or all of the following; QMS, HACCP, legislation, specifications, Technical Reports, Contaminants & Non Conformance Logs, complaints, microbiological & nutritional surveillance, this work includes data entry, trending, filing, information requests, co-ordination of more »

Significant leadership experience in QA. Expertise in regulations and GMP. Strong managerial and problem-solving skills. QP qualification and relevant degree. Familiarity with electronic QMS systems. more »

in an engineering and/or manufacturing environment. Conversant with the process of attaining and maintaining accreditations to ISO 9001 and ISO 45001 Experienced QMS/H&S auditor This is a great opportunity to join a fast growing SME organisation and be a key member of their Senior Management more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of more »

and SME for all compliance platforms, responsible for training users and leading continuous improvement efforts. Lead and represent in validation efforts, ensuring consistency with QMS and corporate policies. Qualifications Bachelor's or Master's degree in Occupational Health and Safety, Construction Management, Engineering, or a related field. Minimum of 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 »

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 »

FID experience (general - Gas Chromatography experience will be considered, to be clear we are looking for someone who has commercial lab experience working to QMS like UKAS 17025 or GLP/GMP/BRC) or GC/MS experience Strong interpersonal, organisation skills Able to work towards deadlines Good IT more »

Management of the destructive and non-destructive testing activity. Management and control of the product and system auditing. Management and control of all relevant QMS systems ISO9001, ISO14001 etc.. Lead and manage the development of preventative/corrective actions. Manage proactively any technical queries with customers providing all necessary guidance. more »

standards, specifically ISO9001 and ISO45001. What you will do: Be responsible for the implementation and ongoing management of an integrated health, safety and quality management system aligned to ISO45001:2018 and ISO9001:2015 requirements, potentially widening to other management system standards over time (e.g. ISO14001:2018, Lead the creation and more »

quality incidents, safety occurrences, and customer complaints, and implement corrective and preventive actions as necessary. Provide support during regulatory inspections, customer audits, and quality management system certifications. What you will need: Strong knowledge of QA methodologies, tools, and best practices including Part 145 Safety Management Systems. Extensive experience in quality more »

friendly team, you will contribute to the continuous improvement of production and development tasks and will have a good understanding of processes working within QMS requirements. As the Quality Engineer you will be responsible for : * The quality of released product and incoming product * Inspecting manufactured components to ensure they meet more »

that arise as quickly and efficiently as possible to prevent compromising quality and safety standards. Ensure compliance and assist with adherence to the Quality Management system (ISO9001/AQAP2110) Report on Key Performance Indicators (KPIs) in order to adhere to process and prevent occurrence of any non-conformity relating to more »

from personal or Sonardyne work activities. To ensure awareness, understanding and adherence to all Sonardyne Policies and Procedures including Health & Safety, Anti Bribery, ISO9001-QMS and Operational requirements at all times. To take an active part in the Sonardyne Continuous Improvement Process, through providing suggestions for corrective actions, suggestions, initiatives more »

To conduct the administrative aspect of the Technical Department taking responsibility for the day-to-day management of some or all of the following; QMS, HACCP, Legislation, Customer Specifications, Raw material specification. · Technical kpi generation and interpretation, including, non-conformance, customer complaints, microbiological performance · Helping to develop and maintain change more »

issues promptly and complete Export Health Certificates as needed. Quality Management Systems: Keep customer online systems updated, conduct GAP analysis, and ensure compliance with QMS, aiming for no customer non-conformances. If you're ready to take on this challenging yet rewarding role in a dynamic environment committed to excellence more »

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 »

Manager and produce month trending technical KPIs Your key responsibilities: Assist in delivery of successful third-party audits (BRCGS). Ensure the site Quality Management System is fully implemented and harness it to drive audit ready standards. Respond to customer technical enquiries. Work with QA Manager and CQA Manager to more »