76 to 100 of 228 QMS Jobs in the UK excluding London

Systems (CDS), Laboratory Information Systems (LIS), Bioinformatics Software, Statistical Analysis Software, Image Analysis Software, Chemical Inventory Management Software, Lab Automation Software, Quality Management Software (QMS), Environmental Monitoring Software, Programmable Logic Controllers (PLCs), Distributed Control Systems (DCS), Supervisory Control and Data Acquisition (SCADA) systems, Human-Machine Interfaces (HMIs), Industrial Control Systems 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 »

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 »

necessary, to ensure that testing is completed in accurate and timely manner. Maintain and review all testing related processes in the department’s Quality Management system to ensure the maintenance and improvement of standards and their continual compliance with ISO accreditation. Maintain laboratory and work areas to ensure they are 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 »

parent company for Eyelit, MESTEC and Optessa who are leaders in Manufacturing Execution (MES), Advanced Planning and Scheduling (APS), Manufacturing Operations (MOM), Quality Management (QMS) and Factory Automation solutions. Eyelit Technologies has delivered unmatched results for a global customer base in the manufacturing industry using cutting edge technology and advancements 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 »

equivalent in a suitable subject Knowledge/experience Essential Evidence of Post-registration laboratory experience (in relevant discipline) Demonstrate active participation in a quality management system to meet regulatory/accreditation standards. Desirable Being able to work as a member of a team Safe handling biological material Skills Essential Team 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 »

he administrative aspect of the technical department taking responsibility of the day to day management and maintenance of some or all of the following: QMS, HACCP, legislation, specifications, technical reports, contaminants, complaints, microbiological and nutritional surveillance. Communication - To ensure effective, professional, timely customer communication. Contribute to customer audits and visits more »

transfer. Duties will be undertaken at City Hospital and Walsall Manor Hospital to NHSBSP guidelines and Sandwell & West Birmingham NHS Trust Quality Managements System (QMS) operating procedures. There is an expectation that the post holder would participate in current shift patterns as deemed appropriate by service requirements. The post holder 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 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 »

Working as a member of a team Special Circumstances Essential Travel to other sites Skills & Knowledge Essential Comprehensive POCT or Blood Science Laboratory Theory QMS (Including Quality control and Assurance) Safe handling of potentially infectious samples Knowledge of health and safety risks & requirements Communication Desirable Interpersonal skills IT (including basic 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 »

the effective deployment of the Integrated Management System (IMS) through internal audits, lead and complete the annual audit schedule, providing assurance that the Quality Management System meets the required standards. Key Responsibilities: Develop and execute a risk-based internal management system audit program compliant with ISO 9001, ISO 14001, and 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 »