76 to 100 of 390 Quality Management Jobs in the UK

UK. They have an interim requirement for a QA Manager to cover maternity leave until November 2024, requirement as follows: Key requirements Experience of Quality & EHS team management with appropriate communication and people skills Excellent knowledge of quality, environmental and H&S management systems and their … application to high technology & engineering environments Comprehensive understanding of the requirements and application of ISO9001 quality standard, ISO 13485 quality systems for medical devices standard ISO45001 Occupational Health & Safety management standard and ISO14000 environmental management standard Qualified auditor Enthusiastic, inquisitive & self-driven individual Ability to work … pressure Track record of high achievement Intuitive lateral thinker with problem solving abilities Attributes Good honours degree in an Engineering discipline Track record in quality management and in the introduction and improvement of quality, environmental and H&S management systems Understanding of mechanical inspection techniques Knowledge more »

company A global leader in industrial automation and instrumentation solutions, mainly to the Process, Oil & Gas, Chemical and Pharma industries, are looking for a Quality Assurance Engineer to join their team on a contract basis. Info about what the role entails Some of the key responsibilities of the role … include: Assist in refining and evaluating the extant Project Quality Management system by establishing requisite protocols, blueprints, and operational directives as necessary. Supervise the enactment of the Asset/Project/Function Quality Management System through periodic audits and evaluations. Provide backing and oversight in implementing … Yokogawas CDM QMS on projects. Generate project-specific quality documentation for client ratification, such as Quality Plans, ITPs, and Databooks with appropriate frameworks. Participate in and furnish input for technical HSE and integrity reviews. Establish and track Key Performance Indicators (KPIs) to assess quality performance across diverse more »

business cases, financial planning and clinical governance where new service developments are proposed. Together with the Head of Nuclear Medicine and the trusts GMP Quality controller act as the Trust expert for the safe use and introduction of all radiopharmaceuticals. Manage specialist staff rotas/leave arrangement to ensure … and manage the service in response to physical environment changes and complex developments including the life-cycling of the unit. This includes the complex management of radioactive materials, external supply, contracts and costs to enable continuing source of these essential materials for the Nuclear Medicine service. Ensure that all … dispensed radiopharmaceuticals for accuracy. Liaise with scientific, medical, nursing and support staff; exchanging very complex information relevant to the patients investigation. Ensure with the quality controller that an effective quality assurance programmes in place. Manage the Radio pharmacy quality management system, ensuring all relevant documentation is more »

Based: Manchester, with hybrid working Term: 12-month full-time contract We are looking for a hands-on individual with extensive project management experience at a Senior Management/Head of Department level, who can plan and deliver a large-scale mobilisation project across 4 sites in Manchester. … As well as relevant experience its likely that youll have formal project management qualifications, such as; PRINCE2, Association of project management (APM), Project Management institution (PMI), Chartered management institution (PMI), Diploma/Certificate in project management, Diploma in project and Quality Management or … Project Management Professional (PMP) certification. Main Responsibilities Determine and define project scope and objectives. Predict resources needed to reach objectives and manage resources in an effective and efficient manner. Prepare budget based on scope of work and resource requirements. Track project costs to meet budget. Develop and manage a more »

finding and repair of high voltage power supplies. 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 product quality and performance issues and raising appropriate non-conformances. Liaising with Design Engineering, Test Equipment Design and Sales in support of meeting customer requirements and finished product quality and performance. Keep informed and support the Company ISO14001 Environmental Management System and ISO9001 Quality Management System and improvement team activities including seeking new green opportunities and suggestions on how the business can improve. Responsibility for adhering to the Companys ISO 9001 Quality, ISO14001 Environmental and Health and Safety management systems. SKILLS, KNOWLEDGE AND EXPERIENCE Ability to test product by following more »

Earn up to £55,000 plus a bonus, working UK-wide as a Project Quality Manager in the thriving solar development sector! Why You'll Love This Role: Competitive Salary & Benefits: Earn up to £55,000 with a car allowance and a KPI-driven bonus of up to 12.5 … holidays. Comprehensive Health & Equipment Provision: Benefit from health cover and full equipment provision, including IT, essential for your role. What You'll Be Doing: Quality Management: Develop and revise quality processes in collaboration with various teams, ensuring top project standards. Subcontractor Coordination: Establish and manage quality requirements for subcontractors, enhancing project delivery. Audit and Compliance: Conduct internal audits, manage non-conformities, and provide quality training to teams and subcontractors. What We're Looking For: Qualifications: Degree in engineering, quality control, or a relevant discipline, with a clean UK driving license. Experience: Robust knowledge more »

QA Operative - Construction We have an opportunity for a Quality Assurance Operative to join our Precast facility in Stewartby, Bedfordshire. The successful candidate will be responsible for but not limited to the following: Maintain document control processes: ensuring appropriate capture and storage of documents, records, and correspondence. Collate and … organise information related to quality assurance. Support the wider site team in daily tasks including the receipt of material deliveries, loading & unloading lorrys and concrete sampling. Ensure that all quality data is accurate and up to date. Implement quality control and assurance procedures to ensure that QA … processes meet the companies established QMS and certification requirements. Assist senior management in preparing for and participate in external audits and regulatory inspections related to quality. As a successful candidate you will be able to demonstrate the following skills and experience: Qualification in a relevant field such as Quality more »

We are hiring a Quality, Risk and Audit Officer who wants the opportunity to carve out a successful role within an award-winning and growing organisation. We have a growing portfolio of clients due to our excellent reputation within the industry and we are seeking to add to our … successful team with an experienced Quality, Risk and Audit officer. We are looking for someone who is motivated to make a meaningful contribution to our business and relish the opportunity to deliver high quality work aligned with their responsibilities. You will be well organised and initiative-taking, calm … to communicate and positively influence and negotiate at all levels, both internally and externally. This role is perfect for an individual with experience in quality management or those that can create and refine internal processes. Key Responsibilities The successful candidate will Contribute and monitor the Quality and more »

shall be responsible for undertaking project engineering duties in accordance with the work package engineering plan, this shall include: Completion of engineering studies and management of consultant engineers. Development of technical specification, review of tender submissions and completion of technical assessments of the bids. Management of Contractor's … Provide assistance in the development and implementation of a project engineering plan. Provide assistance in the development and implementation of a Cable System Risk Management Plan. Coordination and preparation of technical documentation for inclusion within ITT and contract documentation package(s) and for the assessment of the received bids … technical recommendation into the Contractor selection process. Responsible for the preparation and completion of engineering studies as required by the package engineering plan and management of any internal and external services or resources that are required to deliver these tasks. Completion of the package specific interface tasks that are more »

MK Recruit is currently recruiting for a Senior Quality Engineer, We are seeking a dynamic and experienced Senior Quality Engineer to join our client's team in North Lanarkshire on a 12-month maternity cover contract. As a Senior Quality Engineer, you will play a pivotal role … in maintaining and enhancing the quality management system, ensuring compliance with industry standards and regulations, and driving continuous improvement initiatives across our operations. Key Responsibilities: Lead the implementation and maintenance of the quality management system in accordance with AS9100 and other relevant standards. Conduct audits and … assessments to identify areas for improvement and ensure compliance with regulatory requirements. Develop and implement quality control procedures and protocols to monitor product quality throughout the manufacturing process . If this sounds like something of interest please send an updated CV to Leonie Martin more »

CK Group are recruiting for a Quality Assurance Assistant to join a growing Cell Therapy CDMO, to be based at their site in Cambridge on a permanent basis. Your main responsibility will be providing support to the QA team and contributing to regulatory compliance, continuous improvement and management of the Quality Management System. Job Summary: Providing support with administration of the QMS, including non-conformance, root cause analysis and CAPAs. Control of documentation; maintenance of records and use of QMS for document control. Support with internal and external audits. Trending for CAPAs and preparation of … reports. You will have the following experience/qualifications: BSc or MSc in a life sciences subject, or comparable experience. Experience working within a Quality Management System (desirable). Excellent communication skills, written and spoken English. Excellent attention to detail. Apply: It is essential that applicants hold entitlement more »

providing a comprehensive genomics service for patients with known or suspected haematological malignancies. Contributing towards patient care by participating in the provision of high quality genomic analyses of haematological tissues, as part of the South East Haematological Malignancy Diagnostic Service (SE-HMDS) within the South East NHS Genomic Laboratory … optimum patient care. As a clinical scientist your duties will include triage of samples for genomic studies, analysis and reporting of complex genomics results, quality management, training and service development. About us Your development and learning Across the GLH we are equipped to offer support if required to … above, to enable rapid patient treatment decisions. You will ensure work is carried out to a high standard and within relevant target reporting times. Quality : You will be expected to contribute to quality management activities, including compliance with UKAS laboratory accreditation standards, teaching, training and performing audits. more »

the hunt for a brand-new QSM Contractor to join the team on a hybrid, contract basis. The Role: Support the maintenance of the Quality Management System, act as Business Administrator for Veeva eQMS, oversee quality associated records and ensure these activities conform to regulatory requirements. Manage … the controlled document scheme, act as GxP archivist, and deliver QA training activities. duties within Quality function. It is desirable, but not essential for the candidate to have a comprehension of basic Veeva configuration to assist them with troubleshooting issues that my arise and to complete basic configuration changes … Essential: Act as Business Administrator for Veeva QualityDocs, Veeva eQMS and Veeva training. Act as the core subject matter expert for the company document management system, be the primary point of contact for document management queries and represent the system during regulatory and client audits/inspections. Management more »

to GMP and company guidelines. Other key responsibilities will include to: - Qualify, maintain and calibrate all laboratory equipment according to procedures. - Maintain all laboratory Quality Systems and Quality Management Systems. - Write SOPs associated with QC Support. - Raise and support the investigation of deviations and associated CAPAs. - Support … the collection of data for reporting Quality Assurance Performance Indicators. Your Background: You are required to have the following qualifications, skills and experience: - Knowledge of Quality Control, Quality Assurance, Quality Systems, GMP and basic understanding of manufacture and packaging of pharmaceutical products. - Stability testing experience - Hands more »

implementation - Managed end-to-end implementation of at least 2 Telecom projects across OSS, Service Assurance, Service Fulfilment, mediation, Provisioning, etc. - Fault and Performance Management - Service Quality Management - Order Management & Inventory Management - Provisioning/Activation across all types/flavour of service - In-depth knowledge more »

The role of Associate Director, Precision Medicine Quality & Design, will be to support the development and validation of biomarker assays and Precision Medicine Solutions. In addition, they will be responsible for supporting the Head of Precision Medicine Quality & Design in the development of a systematic quality risk … management program for Precision Medicine (PM) across multiple areas, including “fit-for-purpose” assay validation, regulatory risk, human biological samples, data disclosure, anti-bribery and corruption, privacy and most importantly, GCP. The Associate Director PM Quality & Design will ensure Precision Medicine strategies on and operations within programs they … support are compliant with GSK policies and procedures and regulatory requirements. The role covers a wide scope of operational quality and compliance responsibilities, from Ph1 through to launch. As Associate Director, Precision Medicine Quality & Design, you will work effectively in a matrix across PM business functions to ensure more »

Supplier Quality Engineer, Supply Chain, Vendor Management, Engineering, COR5497 The Role This is an excellent Supplier Quality Engineer role, working for a company with a growing reputation in their field. The Supplier Quality Engineer will use prior experience of vendor management, a sound understanding of … the manufacturing space and a strong grasp of Lean manufacturing in-order to ensure a streamlined and organised supplier management process, ensuring the elimination of waste, emphasising defect prevention & reduction of component variation. The successful Supplier Quality Engineer will be based-in the Cambridge office and will be … required to travel UK-wide, with some (though minimal) non-UK travel; therefore a full driving licence is needed. The Company The Supplier Quality Engineer will join a global organisation within the scientific manufacturing industry who are dominating their field. They are experts in the design and manufacture of more »

Senior Manager Global Quality Operations (Senior PV Auditor) This is a home-based role offering a fantastic package including generous salary, incentive bonus, home based allowance plus much more. My client a Global pharmaceutical company are seeking an experienced Senior Manager, Global Quality Operations to manage and perform … audits with focus on Pharmacovigilance audits. Responsibilities include Continuous improvement of the Quality System Pharmacovigilance Audits Inspections - Regulatory Intelligence Provide advice and act as project liaison Skills Degree in natural science or equivalent number of years' experience Experience in Pharmacovigilance auditing KEY RESPONSIBILITIES & DECISIONS 1. Pharmacovigilance Audits · Implement & maintain … internal and external auditees · Maintain a tracking tool for audits, findings and corrective and preventive actions · Select and manage qualified service providers for Global Quality, e.g., contract auditors · Provide business support as Global Quality for routine software/infrastructure lifecycle activities (systems introduction/maintenance/retirement) · 2. more »

clients and candidates, and to create a positive work environment that encourages equality, innovation, and professional growth. Job Summary: As the Senior Manager, Site Quality Assurance, you will play a pivotal role in overseeing and enhancing quality assurance operations at our manufacturing site. Reporting to the Site Leadership … professionals, ensuring compliance with regulatory standards and fostering a culture of continuous improvement. Key Responsibilities: Manage all site-related QA operations in accordance with 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 and monitor quality standards and metrics to ensure compliance and effectiveness. Utilize quality metrics to mitigate risks, enhance more »

Are you ready to take the next step in your career as a Quality Engineer? Look no further! We are seeking a skilled and proactive Quality Engineer to join a progressive Manufacturing business on a permanent basis. This is an opportunity you won't want to miss! As … Quality Engineer, you will support the overall quality function during an exciting period of growth and investment within the company. The role will involve you: Supporting and update the QMS. Leading and conducting thorough audits to maintain and improve quality systems. Utilising ISO systems to drive continuous … improvement in quality management. Monitoring and reporting on quality performance on site. Identifying root cause of quality issues. Implementing corrective actions and new processes. Supporting lean initiatives within the business. Working with internal teams to improve overall processes, developing and implementing SOPs and training teams as required. more »

The role of the QA Compliance Officer is to support governance and compliance of the Pharmaceutical Quality Management System (PQS) at Piramal Grangemouth and maintenance of Regulatory Registrations/Licenses/Certifications. The role will support the site and related functions in maintaining compliance with GxP regulations and … applicable quality guidelines, including, but not limited to UK/EU/US GMP/GDP, ICH and other region specific guidance. The individual will have support key quality system elements and compliance improvements, working closely with relevant stakeholders on site. Role •Supporting key quality system elements … tracking of site compliance commitments and follow up actions. •Working with the wider site functions to drive down out of compliance events and implement quality improvements •Support and track regulatory findings and trends that may lead into a focus of regulatory inspections •Support review of procedures and other QMS more »

person to lead the delivery of radiotherapy services within our Cancer Centres in Newcastle and Carlisle (Northern Centre for Cancer Care North Cumbria. This management position within NCCC/NCCCNC involves the full range of management accountabilities including day-to-day operational management of the radiotherapy department … vacancy. Please expand the job details section and read all of the information before applying for the vacancy. Main duties of the job This management position within NCCC/NCCC-NC involves the full range of management accountabilities for the delivery of radiotherapy services, including day-to-day … operational management of the departments in both Newcastle and North Cumbria. A key objective for the post holder is to ensure equity of service delivery across the geographically spread treatment locations. This requires the post holder to ensure effective agreement exists between the departments in delivery of both strategic more »

Quality Assurance Cheadle (SK3) Monday to Friday, Days £30,000 - £36,000 Starting Salary Benefits Excellent Pension Life Assurance Bonus Scheme 25 Days Holiday + 8 Days Bank Holiday I am working with a global manufacturer that has invested hugely in growing it's quality function in the … last 6-12 months. An excellent opporutnity has arisen for a Quality Professional with strong manufacturing experience and excellent customer facing skills to join a developing team. This opporutnity offers excellent long term growth and progression. Role Description Engage with customers and key stakeholders to the business Determine route … cause analysis and implement corrective actions Perform internal audits Quality Management for suppliers Train wider teams on quality procedures Support quality improvement programs Skills and Qualifications Experience working within manufacturing. Customer facing experience 8D Management experience Knowledge of quality standards Company Information As a more »

of care devices for the international market. Due to rapid expansion they have a position for a 12 month fixed-term contract with the Quality Engineering department. There is potential that this may turn into a long term position. The role offers Hybrid working for those not close to … site. Position Reporting to the Quality Lead, the successful candidate shall be accountable for maintaining compliance of the Quality Management System, input into the management of complaints and post-market activities ensuring that the requirements of ISO 13485:2016, CFR 21 Part 820 IVDD/IVDR … are adhered to. The successful candidate shall be responsible for carrying out day-to-day Quality Management Systems and post market activities associated with the on-market product. Activities such as document creation and review, input into and performing investigations, vigilance reporting and maintenance of trend analysis are more »

Quality Engineer Lead, Scientific Instrumentation Basic Salary £35,000 to £46,000 Bonus 10% Pension Healthcare Life Insurance Holidays The Role - Quality Engineer Lead , Scientific Instrumentation Our client is looking to recruit a Quality Engineer Lead responsible for: Maintaining ISO accreditation and improving the quality management system performance Supporting a reduction in supplier quality problems and non-compliance on shop floor quality Assisting in the development and implementation of good fit processes Your Background - Quality Engineer Lead, Scientific Instrumentation To succeed in this varied and exciting role you must be able to … demonstrate the following: Background in a similar role, working as a quality engineer or quality lead Good understanding of quality focused high technology and the manufacture of complex equipment Excellent verbal and written communication skills The Company - Quality Engineer Lead , Scientific Instrumentation Well respected supplier of more »