1 to 25 of 253 QMS Jobs in the UK

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 »

You will be required to support the Head of QA, responsible person and responsible personfor import, in the implementation and maintenance of the Quality Management System in accordance with ISO 9001 and ISO 13485 standards, and in compliance with EU GDP guidelines. Ideally you will have experience of working in more »

or exceeding of SLAs and KPIs. Adhere to all company policies, procedures and business ethics codes including anti-bribery policy and Environmental and Quality Management System (compliant with ISO 9001 and 14001). PERSON SPECIFICATION Required skills and experience ERP Systems Expertise: In-depth knowledge and understanding of Dynamics more »

of the relevant regulations Provide reports to management to enable them to monitor system performance. Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. Identify and collaborate in the implementation of changes more »

of the relevant regulations Provide reports to management to enable them to monitor system performance. Review and authorise documentation and processes in the Quality Management System to ensure compliance with established quality procedures and applicable regulations and alignment with other related documentation. Identify and collaborate in the implementation of changes more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

and working with suppliers to arrange processing and shipment of critical devices. There will be some involvement with supporting other areas of the Quality management System as outlined in the Key responsibilities below. Key Responsibilities Ensure compliance with ISO 9001 Quality, ISO 14001 Environmental, and ISO 45001 Health and Safety more »

systems and assurance, with relevant QHSSE experience in a manufacturing and/or project environment. Experience in the implementation and maintenance of a Quality Management System/ISO certification is essential. You are well organised, with good analytical and critical thinking skills, and excellent verbal and written communication skills. You 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 »

and Flow Cytometry section. 2. To help support managerial responsibility for all coagulation analytical platforms and associated assays. 3. To help deliver and maintain QMS to comply with UKAS (ISO15189) standards in the specialist area. 3. To help ensure HR policies and procedures are effectively managed within Blood Sciences-Haematology. more »

prevent occurrence. Reduction in Quality Management System (QMS) non-conformances, and Customer Complaints & repeat process NC's. Timely implementation of product, process, and Quality Management System changes. Avoidance of product recalls. Compliance with approved procedures. Adherence to the QMS, GxP & Regulatory requirements. Develop, generate, and maintain documentation to support an … effective and compliant QMS, including: Product Routers & Assemblies (PRA), Material (DRM) and Product Specifications Product and Process FMEAs/Risk Assessments Customer Complaints Medical Device Risk Management Reports and Files Quality Inspection Procedures and Control Plans Quality Systems and Process SOPs and Work Instructions (PWI). Conduct internal Audits, GMP more »

for Daily Management of the Functional team and their performance; Leads people using company values and core behaviors with a GEMBA presence. Maintain Quality Management System in accordance with Corporate, BU and regulatory requirements advocating complainant change management. Leads and implement strategic initiatives to reduce the number of internal and more »

Procedures, Training Instructions and Batch Records. This includes document review and approval. Perform CAPA Coordinator activities; coordination Quality Incidents and Deviations within a Quality Management System (Agile. Proactively contributing to continuous improvement initiatives and other general housekeeping duties. Taking a self-motivated approach to continuous professional development and engaging with more »

programme Maintain network of external audit providers to support CMC, pre-clinical and clinical activities. Support the management, implementation, and maintenance of the Quality Management System to support clinical development activities. Support senior management in providing direction and leadership to staff to ensure a quality mindset is embedded in the more »

Manager. Familiarize Yourself with ISO 9001 Project Plan Identify Responsibilities, Policies, and Objectives of the Project Develop Your Project Documentation Up to Launch Quality Management System Review Performance Register for Certification Continual Improvement activities Key Responsibilities – Project Manager Quality Systems Promote Health and Safety in the workplace above everything else more »

to deliver our service commitments. Highlighting any non-conformances to the relevant personnel. Supporting the QA team to include all parts of the Quality Management System that is in place to ensure we continue to develop activities and policies aimed at improving the effectiveness and efficiency of the service. The more »

range of responsibilities and duties with this role, as the Quality Assurance Engineer will be responsible for managing the EN9100 internal audits, maintaining the QMS, supporting continuous improvement and evaluating risk. The Quality Assurance Engineer will also be responsible for completing CAPAs with the audit team and participants. They will more »

to organise group training sessions using Microsoft Outlook Calendar/Scheduling Assistant. * Ability to compile PowerPoint presentations to cover training topics related to the QMS· * Ability to confidently interpret and present PowerPoint presentations prepared by others. * Ability to chair meetings and take scribe notes from those meetings. * Microsoft Excel Skills more »

levels of GMP, food safety and integrity standards. Responsibilities Include: • Supporting the overall technical strategy, tactics, policy & plans • Responsible for the company’s quality management system to ensure compliance with standards and (HACCP) procedures on food handling • Coordinate all quality assessment and laboratory activities • Ensure that both inbound and outbound more »

and completing corrective actions required to address any areas of poor performance, including, where required, staff performance management. Ensure all documentation required for Quality Management System is recorded and maintained Communicate efficiently, courteously and with clarity at all times, whether face to face, telephone or electronic methods referring enquiries to more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

as performance management, absence management, measuring results and how to have regular conversations. Adherence to Company policy and working to the company ISO Quality Management system (9001 certification) and company security management system (27001 certification in the UK) at all times. Work with the wider global HR team to ensure more »

throughout our business and ensure we deliver the optimum level of efficiency whilst maintaining the highest quality standards and continuous improvement of our quality management system ISO 9001:2015. We aim to minimize environmental impact of our own systems and help develop environmentally responsible customer solutions. DPS Group recognises its more »

high voltage power supplies to specification requirements. 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 »

manufacturing engineering, or similar. Experience in process and product validation (sterile packaging according to ISO 11607 would be advantageous). Understanding of a quality management system (ISO13485/FDA) and medical device manufacturing advantageous. Very good MS-Office skills, especially Excel. Strong organizational skills with the ability to communicate at more »