76 to 100 of 223 QMS Jobs in the UK excluding London

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 »

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 »

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 »

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 »

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 »

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 »

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 »

across various departments, including NPD and Operations. Experience working within an environment that Exports would be beneficial Technical Manager Qualifications and experience: BRC experience QMS experience HND or degree (or equivalent) in Food Science/Technology or similar Previous experience working in a similar role This is very much a 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 »

awards, refer a friend recruitment. This role would suit candidates who have previously worked in roles such as Technical Services Manager, Compliance Manager, Auditor, QMS manager, Quality Systems Manager, Supplier Assurance Manager, Technical Manager. This role is located between Taunton and Exeter just off the M5 more »

development, and operational efficiency. Directly manage employee appraisals, recruitment efforts, SLA compliance, and round-the-clock support schedules. Key Responsibilities: * Champion our clients Quality Management system, ensuring adherence to procedures and consistently high service levels for our clientele. * Provide proactive and reactive technical support to our customer base, resolving issues more »

compliance. Contact suppliers to resolve price, quality, delivery, or invoice issues. Support and adhere to policies, procedures, and operational guidelines related to established quality management system (IATF 16949). Maintain a working knowledge of safety policies and regulations to ensure duties of self and others are performed in a safe more »