101 to 125 of 275 Permanent QMS Jobs in the UK

lab analysis Working closely with other sites for product specifications and documentation. Dealing with external stakeholders for food safety, quality and importing Maintenance of QMS Experience & Skills Required: The business is looking for an individual who has experience within the food industry. You must be able to lead, motivate and more »

lab analysis Working closely with other sites for product specifications and documentation. Dealing with external stakeholders for food safety, quality and importing Maintenance of QMS Experience & Skills Required: The business is looking for an individual who has experience within the food industry. You must be able to lead, motivate and more »

standards. Responsibility for all food quality, ensuring that safety and assurance are measurably maintained to best standards by system audits and improvements were required – QMS and HACCP Manage the HACCP/TACCP team. Has overall responsibility to ensure all customers, Halal, food technical and certification standards to satisfy the customer 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 »

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 »

Overview: To ensure that all the products produced are assessed in accordance with the companys and customers requirements, the site Quality Management System and HACCP System, in order that the quality, safety and legality can be assured and that all the necessary information is accurately recorded and retained The Position more »

considered) Work Timings : US Timings (EST -3 days and PST -2 days) Job Responsibilities- 1.Compliance with working SOPs within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. 2. Implement and follow the latest versions of CDISC, FDA Guidelines, GCP 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 »

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 »

socially and professionally, with regular post-work events and regular group lunches. There is an atmosphere of openness and collaboration. We have a quality management system annually certified by the BSI to allow us to develop Software As a Medical Device, we have a machine learning operations created in-house 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 »

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 »

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 »

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 »