1 to 25 of 44 Permanent Quality Management Jobs in the East of England

outcomes for our customers the Group has seen steady growth and expansion. We now have exciting permanent opportunity for a motivated and suitably qualified Quality Management Lead. Join us and be part of making a valuable contribution to Sizewell C- a proposed new nuclear power station that is … targeted to start construction in 2024. Job Summary: The role of the Quality Management Lead (QML) is to ensure Sizewell C (SZC) quality requirements are complied with across the full project life-cycle (Contract award, Design, Procurement, Manufacture, Test, Shipping, Construction/Installation, Test/Commission and … Contract close out). Principal Accountabilities: Support the development of quality (QA/QC) arrangements for deployment across the SZC organisation; Implement key quality arrangements related to the following topics: Manage Quality Execution Support Technical Assessment of Suppliers Conducting & Modulating Manufacturing Surveillance Management of Non-Conformance more »

Reporting to the Group Quality Manager (who is also our Group Data Protection Officer), the Regulatory & Quality Engineer ensures that the company's quality policy is implemented and respected, and plays a pivotal role in matters relating to the Quality Management System. Operating in an … ordinate customer audits , including scheduling, preparation, execution, and follow-up activities. Conduct regular internal audits to identify areas for improvement and ensure adherence to quality standards. Manage the process of responding to customer questionnaires and feedback, ensuring timely and accurate responses. Contribute to the supplier qualification processes, including conducting … supplier audits and assessments to evaluate supplier capabilities. Maintenance of the QMS: Contribute to the creation, maintenance, and organisation of quality-related documentation , including SOPs, work instructions, quality manuals, records and training material. Establish key performance indicators (KPIs) and metrics to measure and monitor quality performance throughout more »

from renowned companies who are leaders in their specialised field. The Role They are now looking for an experienced QMS Administrator to ensure the Quality Management System processes are established, implemented and maintained. Key Accountabilities Implement and maintain the companys quality management system (QMS) to ensure … with ISO 9001 and other relevant standards. Perform regular audits of processes, products and services to identify areas of improvement and ensure adherence to quality standards. Develop and maintain quality documentation such as procedures, work instruction and quality records to support the QMS. Monitor and report on … quality performance metrics to senior management, highlighting trends, risk and opportunities for improvement. Manage and resolve customer complaints related to quality, documenting issues and taking actions to prevent recurrence. Manage the internal audit, KPI Metrics and annual recertification with LRQA. Consistently identify areas of improvement, supporting the more »

to become more cost-effective and scalable, allowing personalised therapies to be affordable for more people. To commercialise their technologies, they are recruiting a Quality Manager to lead them through ISO 9001 and other regulations. This would include developing and building quality frameworks for all stages of project … development and manufacture through the management of a digital document quality management system (QMS). This will require good communication skills to get buy-in from all stakeholders. Requirements: Graduated with a bachelor's or master's in engineering or similar. Substantial demonstrable experience leading a company …/13485 relating to medical device instrumentation development and manufacture. Further exposure to GMP manufacture for biological products would be desirable. Comprehensive experience with "quality management" within a technology company including instilling a quality-focused culture and maintainable approach to quality processes. Detail oriented and strong more »

complex systems for use in the defence sector globally. This is a fantastic opportunity to join a company that pride themselves on delivering high quality superior products to their sector. Job Role – Principal Product Assurance Engineer (Supply Chain) The Principal Product Assurance Engineer shall join the Quality Supply … Chain team in support of non-conformance management and audit of the production supply chain. Duties – Principal Product Assurance Engineer (Supply Chain) • Handle major equipment supplier Product Non Conformance. • Facilitate implementation of the non-conformance defect investigation process with the supplier to ensure that adequate and appropriate corrective actions … are implemented. • Provide supplier Non-Conformance data analysis and summary reports. • Identification of improvements with respect to the supplier non-conformance management process and its implementation within SAP. • Conduct Quality audits/assessments. • Opportunity to identify process improvements to aid on time and on quality delivery of more »

Compliance/Quality Administrator – Medical Devices We are looking for a Compliance/Quality Administrator to join a dynamic company developing an array of products for the medical and healthcare industry. The company is growing and offering many opportunities for personal career development in addition to a wide … variety of new projects to work on. As the Compliance/Quality Administrator you will join their Product Management Team and will be responsible for document control in compliance with applicable regulatory standards. The job will suit a friendly, diligent and motivated individual with a background in Quality Assurance/Quality Management/Document Control or similar technical administration role within medical equipment sector. Compliance/Quality Administrator`s Responsibilities: Producing, updating and maintaining product specifications and design documentation, making sure that all documentation complies with internal procedures and International Standards. Manage product changes more »

relocation package may be available. Our vision is to deliver innovations, high-performing pathology services that is focussed on our customers and delivers high quality and fully compliant services. We are clinically led and designed to achieve the benefits of scale that can be achieved by working together to … Grifols analysers in blood transfusion, blood track and Contronics temperature monitoring system. In haematology and coagulation we have Sysmex XNs and ACL TOPS. For quality management we use Q-Pulse system. We are also in the process of upgrading our existing LIMS system (winpath enterprise). Main duties … of the job About our Pathology Service Specialist Biomedical Scientist Job Information You will enjoy a varied range of responsibilities from maintaining the quality management system and UKAS accreditation, training of less experienced members of staff, validating and authorising results and most importantly providing quality service for 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 »

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 »

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 »

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 »

they are seeking to employ a Technical Manager to start as soon as possible on a permanent basis. You will have: Experience in a Quality assessing field previously Have a good knowledge of HACCP TACCP & VACCP systems Understanding of trace testing Strong Excel knowledge and skills Attention to detail … quality controlling Experience within BRC - Supply chain assurance Must have experience in running a QMS Working Hours: Monday Friday 8am 4pm or 9am 5pm Role Overview: Be the technical and compliance contact for their customers, service providers and their growing team Advise the product development team of all relevant … food safety guidance and legislation Ensure product packaging compliance Liaise with team members on all matters related to product quality and report back to the relevant people when required Complete inbound product checks of all raw materials Provide additional QC support during production runs Responsibilities & accountabilities: (list key tasks more »

of the role: Providing leadership and expertise, and setting policy, in the science, technology, and operation of the transfusion sections of the two laboratories Management of staff including recruitment, provision of training, management of employee performance, absence management, and management of rostering Accountability for the clinical … safety of the transfusion service, and operation of the quality management system, including compliance with the Blood Safety and Quality Regulations 2005 (as amended) and BS EN ISO 15189:2012 Liaison with the client, Mid and South Essex NHS Foundation Trust, and their partners, through participation in … formal meetings, especially the Hospital Transfusion Committee, and consistently achieving contractual performance targets. Oversight and management of information assets, especially the transfusion module of the Clinisys WinPath system and its interconnected systems The procurement and management of supplies and equipment for transfusion The health and safety of employees more »

and ensure a safe working environment for all employees. Key Accountability The engineer will ensure that we meet the requirements set out in our Quality Management System while ensuring that health and safety is a priority. Ensure that documentation (service reports etc) are completed and stored in the … of safety protocols and the ability to respond to emergencies. Experience of maintenance repairs, such as electrical, and plumbing. To have an understanding of Quality Standards such as ISO13485, ISO9001, ISO14001 or other applicable standards, working with a Quality Management System. Ability to work independently and manage more »

upcoming product lines. Your duties will involve testing a diverse range of devices, creating effective test methods and fixtures, and ensuring strict adherence to quality standards. Key Responsibilities:Contribute to the V&V process for new product development, including testing various devices and designing appropriate test methods and fixtures.Write … protocols, document procedures, 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 … s degree in Electronics or Mechanical Engineering.Up to 5 years of proven experience in testing equipment and product development.Strong understanding of regulatory requirements and quality management systems in the medical device sector.If you are having difficulty in applying or if you have any questions, please contact Jaeme Pawl more »

upcoming product lines. Your duties will involve testing a diverse range of devices, creating effective test methods and fixtures, and ensuring strict adherence to quality standards. Key Responsibilities: Contribute to the V&V process for new product development, including testing various devices and designing appropriate test methods and fixtures. … protocols, document procedures, 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 … in Electronics or Mechanical Engineering. Up to 5 years of proven experience in testing equipment and product development. Strong understanding of regulatory requirements and quality management systems in the medical device sector. If you are having difficulty in applying or if you have any questions, please contact Jaeme more »

MHRA and Home Office. Leading and closing any audits performed by the above authorities, or per customer/client. Monitoring and investigating trends in quality KPI's, namely fails, rework and complaints and report to the Board. Leading a culture of continuous quality improvement by constant monitoring and … review of the Quality Management System. Promoting and educating colleagues in GMP (Good Manufacturing Practices) and GDP (Good Distribution Practices). Acting as Quality authorisation, signing off in conjunction with the Quality Director. Developing a strategy for the Quality Department with the Executive Directors to … ensure continuous regulatory compliance whilst supporting business development and meeting board objectives. Providing Aseptic Quality input into the Management Review ensuring outstanding issues are actioned and resolved, reporting to the Board if necessary. Providing quality information to other departments as required for new customer business, product, and more »

the short application form on our website. We’re interested in hearing from candidates with experience in the following areas: Key Account and Product Management Quality Management Mechanical Engineering Mechanical Design Electronics Engineering Mechatronics Engineering Software Engineering (industrial automation, embedded) Verification and Validation Engineering Cellular Origins Cellular more »

Quality Compliance Engineer - RF | £40k-£45k DOE | Chelmsford | Permanent We have an exciting opportunity for a Quality Compliance Engineer to work on production equipment used for the manufacture of RF products, from standard to bespoke solutions. Our client is known for being at the forefront of technology and … with a solid understanding of relevant regulations and standards, and how to meet them from an electrical and mechanical design perspective. Emphasis on Product Quality: Ensure RF Power systems, processes, and products operate correctly and consistently. Track, monitor, and report on non-conforming processes and products, overseeing the execution … of all relevant Corrective Actions, Deviations, and Quality Notifications. The responsibility of a quality compliance engineer is to guarantee that, through efficient monitoring and control, customer expectations are met or exceeded. In the event that an escape occurs, the engineer also makes sure that the proper root cause more »

The role As QHSSE Coordinator you are responsible for SEA-KIT s Quality, Health, Safety, Security and Environment (QHSSE) guidelines and for ensuring that the company is in compliance with published policies, supporting standards and legislative framework. You coordinate and lead the QHSSE assurance activities for SEA-KIT, ensuring … and practices are identified, developed, implemented and adhered to across SEA-KIT s design, build, testing and commissioning operations. Define, lead and oversee all Quality processes in SEA-KIT s design, build and testing of its products. Perform quality checks and instigate problem solving to investigate and resolve … any issues identified. Review non-conformances identified during the build/fit-out and testing of SEA-KIT s USVs to improve the quality of the vessel design and build. Lead the company s ISO 9001 annual recertification, and oversee external reviews and audits to maintain certification. Lead the more »

s Hospital and the Rosie Hospital in Cambridge. With over 12000 staff and over 1100 beds the priorities of the Trust focus on a quality service which is all about people - patients, staff and partners. Recognised as providing 'outstanding' care to our patients and rated 'Good' overall by the … Care Quality Commissioner, is testament to the skill and dedication of the people who work here. CUH's values - Together - Safe, Kind, Excellent - are at the heart of patient care, defining the way all staff work and behave. The Trust provides accessible high-quality healthcare for the local … Academy for Healthcare Science (AHCS). Skills Essential Able to concentrate for prolonged periods and able to work under pressure Good organisation and time management skills Team working Computer literate - MS Office Good verbal and written communication Desirable Communicating with external suppliers Knowledge Essential Knowledge of relevant health and more »

The post holder will also be the lead Team manager for overseeing the implementation of future projects in addition to the day to day management of Digital Histology. This role will be working with and supported by the senior Histology Management Team. Main duties of the job The … the role are outlined below: To provide a highly specialist level of theoretical and practical Histopathology knowledge To work as part of a core management team for Histology with other Team Managers and provide technical leadership. To carry out tissue dissection to IBMS/RCPath standards in specimen categories … within competence and as agreed with consultant staff. To work as part of a core management team for Histology to ensure regular audits are performed and acted upon appropriately. With Support and guidance, implement Digital Pathology in an efficient and timely manner at both Southend and Basildon Histology Sites. more »

ingenuity of its 7,250 people in the UK & Ireland, to deliver extraordinary outcomes for its clients. We currently have an opportunity for a Quality Assurance Engineer to join our Altrad Babcock team at Sizewell B Nuclear Power Station. To be eligible for the role you must hold CTC … the correct standards and show a positive attitude. Ensure safety of people and the environment. Have knowledge and familiarisation of associated mechanical, civils and quality procedures. Customer Satisfaction is achieved by understanding & exceeding clients’ needs and expectations in order to make their business a success. Scope, Time and Cost … required proactive mitigation is evident. Ensure high standards of workmanship within the facilities. Always use best practices & continually look for innovations that support continuous quality improvement. Continuous Improvement tools and techniques are deployed to improve efficiency and effectiveness for both Altrad and the Client. Absence management and timekeeping more »

unique opportunity to expand your network and understanding of the organisation. You'll be actively engaged in a multinational project, working alongside an established Quality network to prevent or minimise product non-conformance, facilitate smooth equipment delivery, guarantee the reliability of products in production, and continuously enhance customer satisfaction. … This role offers the chance to join a dynamic quality organisation and enhance your skills as a quality professional. You will have the opportunity to learn and implement the latest quality tools and techniques, contributing to the identification of process improvements that ensure timely and high-quality product delivery throughout the product lifecycle. Additionally, you will be responsible for managing quality assurance activities across an international supply base. What we’re looking for from you: An engineer with a strong background in quality management systems, techniques, and processes, particularly during industrialization and manufacturing more »

Job DescriptionRRxCo is partnered with a leading Life Science Manufacturer in the search for a UK Head of Quality to support significant growth. They are seeking an experienced leader to drive standards as a top-tier Life Sciences manufacturer. You will lead Quality advances across their team of … colleagues, build a dedicated Quality team in the United Kingdom (UK), and grow a culture of world-class quality.DeliverablesDevelop, implement and manage the Quality system and strategy, to ensure it meets the business requirements and customer deliverables.Lead, manage, and recruit an effective Quality team ensuring compliant and … work with the wider business to deliver and sustain ISO9001:2015.Build and refine a fit-for-purpose supplier assurance model whilst implementing effective risk management processes and tools.Introduce and mould a best-in-class Quality culture whilst maintaining and improving the effectiveness of the business.Support and lead as more »