1 to 25 of 221 QMS Jobs in England

highest standards of quality and compliance in all aspects of our operations. Job Description: We are seeking a highly skilled and experienced Site Lead (QMS) to join our team. The Site Lead will be responsible for ensuring compliance with regulatory requirements, overseeing MHRA client audits, managing our global Quality Management … System (QMS), and implementing a labelling service. Key Responsibilities: Develop, implement, and maintain a comprehensive Quality Management System (QMS) to ensure compliance with regulatory standards, including MHRA requirements. Lead and manage MHRA client audits, ensuring timely preparation, coordination, and follow-up activities. Develop, implement, and maintain the Quality Management System … interacting with regulatory agencies. Strong knowledge of global regulatory requirements, including MHRA regulations, FDA regulations, and ISO standards. Experience developing and implementing Quality Management Systems (QMS) in a global environment. Preferred Qualifications: Experience implementing labelling services or managing labelling operations within a regulated industry. Certified Quality Auditor (CQA) or equivalent more »

have a wide range of responsibilities, from operational tasks like batch review and production liaison to broader activities such as auditing, supplier management, and QMS implementation. Crucially, you'll also serve as Deputy QA Manager, with some immediate line management duties and close collaboration with the QA Manager to meet more »

risk. Oversee and direct the complaints process, ensuring timely resolution and ensure effective communication with relevant departments. Safeguard and promote the integrity of the QMS to ensure compliance to EN9100. Develop and provide training to staff on internal quality processes, standards, and best practices. Ensure the protection of Company Intellectual more »

in our manufacturing and operations teams. Key areas of responsibility: Validation of changes to Manufacturing & QC standard operating processes Document control within a Quality management system to ensure traceable, logical and consistent workflow and procedures. Liaise with appropriate departments to contribute to the rapid and effective investigation of process quality more »

for improvement. Collaborate with manufacturing engineers on customer requirements to ensure compliance within the Production environment. Assist in general Upkeep & continual improvement of the QMS to ensure compliance to EN9100. Develop inspection and risk management methods to analyse product quality inline with customer requirements such as MSA, FMEA, CPK. Perform more »

responsibilities will be: Develop and implement quality assurance policies, procedures, and standards specific to defence and naval systems. Establish and maintain a comprehensive quality management system to ensure consistent product quality and reliability. Lead and manage a team of quality assurance professionals, providing guidance, training, and support as needed. Collaborate more »

responsibilities will be: Develop and implement quality assurance policies, procedures, and standards specific to defence and naval systems. Establish and maintain a comprehensive quality management system to ensure consistent product quality and reliability. Lead and manage a team of quality assurance professionals, providing guidance, training, and support as needed. Collaborate more »

Overview: Support the quality team with co-ordinating and conducting internal audits in accordance with the internal audit plan, assist with maintaining the quality management system across all departments. Identifying areas for improvement of internal processes to meet and exceed industry standards and customer expectations. Key Responsibilities: Perform audits of more »

to customers Actively participate in document control Direct interaction with customers on quality issues Undertaking Continuous Improvement activities to ensure the integrity of the QMS is maintained Person Specification A-C GCSE Level or equivalent in English and Maths Manufacturing or Operational qualification or relevant proven experience HNC or Degree more »

systems and impact assessment of pertinent change controls. Any other assigned duties. Requirements: Experience with TrackWise, LIMS and Documentum and/or any other QMS systems. Acquaintance global GxP, e.g., FDA CFRs, EU, 'Third countries' other than the UK. Familiarity within a pharmaceutical manufacturing, testing or quality assurance setting in more »

Infrastructure, Manufacturing, Chemical, Education and Training, Healthcare, Pharmaceutical, IT, Finance, HR and Support Services markets. We offer this service through the Ten Live Quality Management System which has combined our 60 years + experience in the industry, our partnerships with industry bodies and regulators and a customer-centric quality management more »

that all costs are considered. Providing routine internal commercial and progress reporting in accordance with management time requirements Maintain systems to see that Quality Management System ISO 9001 and 14001 are implemented. Progress all sales opportunities. Develop and pursue new and existing sales leads Ensure No Claims are made on more »

or maintaining and archiving documentation Supporting and executing external audits where applicable Supporting management when hosting regulatory audits Working on executing and maintaining the QMS, including but not limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls OOS/OOT The Person: Will have a Degree in a relevant more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

or Quality Manager or Quality Management experience gained within a software development working environment. Experience of ISO9001:2015 quality standard and maintaining a Quality Management System Any knowledge or experience of ISO27001/002 or maintaining an Information Security Management System would be advantageous but not essential. Experience of developing more »

related meetings. Maintaining the divisions central quality and service management documents, which includes conducting regular reviews and updates to policies and procedures. Maintaining the QMS and SMS risk and action logs. Liaising with external and internal auditors, including issuing and reviewing audit reports, maintaining audit finding logs, and proactively following more »

regulations. quality performance metrics, targets, and KPIs to monitor and drive continuous improvement initiatives. Quality Assurance Strategy implement, and maintain robust aviation-specific quality management system in accordance with industry standards and regulatory requirements. effective documentation control, recordkeeping, and configuration management processes to maintain the integrity of quality records and more »

Quality Agreements and GMP guidelines. Serve as the QA representative on the Site Leadership Team. Lead adherence to local or corporate Quality Management Systems (QMS). Collaborate in developing the Quell PQS, including implementing an eQMS where applicable. Define and develop new quality processes, policies, and data management systems. Establish more »

in resolving equipment problems and proactively preventing performance issues. Assist commercial, procurement and legal teams with quality-related tasks. Implement and update project quality management system (PQMS) according to ISO standards to meet the ever-evolving BESS business development and project quality needs. Cultivate and exemplify a quality culture that more »

the development and validation of biomarker assays and Precision Medicine Solutions. Facilitate/participate in projects to deliver improvements to the clinical laboratory Quality Management System through collaboration with R&D Understand the business needs of PM departments, with respect to technology infrastructure, third party work and human biological sample more »

facilities in the UK and abroad Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System, compliant with ISO standards PERSON SPECIFICATION Required experience Experience of working in a similar technical engineering role related to electrical networks, solar, battery storage more »

Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in accordance with the relevant processes (e.g. Quality Management System) To monitor project and/or support activities to ensure systems are fit for purpose, that significant risks are identified and mitigated, and that more »

expert who is fully versed with Samsung processes and platforms 10+ years of experience in Project management/Vendor Management with good knowledge in QMS systems HOURS OF WORK: 37.5 hour week. Some weekend and evening work may be required for emergencies and projects. CHALLENGE: We are operating in a more »

Computerized Systems Validation and knowledge of ISPE's GAMP and FDA 21CFR Part 11 would be advantageous. Adherence to SOPs and experience with a QMS will be required. The ideal candidate will have a life-science degree or similar with good communication, planning and organizational skills and be a strong more »

which utilise the databases provisioned. -Preparing and delivering regular reports in relation to database performance, trends, and improvements. -Ensuring all documentation complies with ISO9001 QMS and best practice. -Ensuring the team have the appropriate resource levels to deliver business outcomes. Required Experience -Degree in Computer Science, Information Technology, or a more »