1 to 25 of 29 Permanent QMS Jobs in London

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 »

also be considered. At least five years of quality management experience and a track record of supporting businesses on their quality agenda. Experience in QMS implementation, HACCP and Trade Associations promoting good food quality business practice. A passion for delving deep to gather all the information available to support identifying more »

High levels of commitment to customer service. Strong written and verbal communication skills. Organisational skills to track and trend performance. Quality-minded focus/QMS experience. Our global team: We are a team of 66,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of whats more »

actively participating in their resolution to maintain quality standards. Track, assess, and approve Non-Conformances (NCs)/Incident Reports (IRs) through the electronic Quality Management System (eQMS), driving continual quality enhancement. Review and approve Quality Documents to ensure adherence to ICH-GCP standards and process improvements, leveraging the eQMS. Prepare more »

team. Other essential responsibilities include: Management of GMP and GDP compliance Management of complaints, CAPAs, risk assessments, and validation protocols Review and manage the QMS system Able to manage non-compliance issues and escalate when needed Have experience in the management of recalls Deal with customer, supplier, and vendor approvals more »

of a global team.Other essential responsibilities include:Management of GMP and GDP complianceManagement of complaints, CAPAs, risk assessments, and validation protocolsReview and manage the QMS systemAble to manage non-compliance issues and escalate when neededHave experience in the management of recalls Deal with customer, supplier, and vendor approvals, including periodic more »

manuals ' Electrical fault finding ' Electrical safety testing ' Provide technical assistance to service engineering team ' Work within and contribute to the company's ISO9001 quality management system ' Liaise with shop-floor to ensure machines are built to appropriate Company standards ' Assist in commissioning of machines ' Any other duties and responsibilities commensurate more »

with regulatory standards, maintaining quality systems, and supporting continuous improvement initiatives. Responsibilities: Support the implementation and maintenance of the company's Quality Management System (QMS) in accordance with regulatory requirements. Assist in conducting internal audits to assess compliance with GMP/GDP standards and company policies. Participate in the review more »

socially and professionally, with regular post-work events and regular group lunches. There is an atmosphere of openness and collaboration. We have a quality management system annually certified by the BSI to allow us to develop Software As a Medical Device, we have a machine learning operations created in-house 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 »

quality incidents, safety occurrences, and customer complaints, and implement corrective and preventive actions as necessary. Provide support during regulatory inspections, customer audits, and quality management system certifications. What you will need: Strong knowledge of QA methodologies, tools, and best practices including Part 145 Safety Management Systems. Extensive experience in quality more »

with existing and new requirements. Specify audit scopes to ensure compliance with legislation, industry standards, and company policies. Maintain and enhance the ISO9001 Quality Management System and ISO14001 Environmental Management System. Approve engineering change documents and concessions, and monitor safety performance of fleet personnel and contractors. Ensure depot staff are more »

prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO 13485 quality management system and collaborate effectively with other engineers to support research and development initiatives and the overall project goal Better patient outcomes! What skills and experience more »

the team and with external partners. 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 Good understanding of communications, wiring systems and schematics or equivalent Experience with inspection and testing– C more »

PDA reports ensuring that it is correctly completed and procedures are followed within the required timescales - Work in line with the Company’s quality management system, industry standards and regulations and Health & Safety policy - Understand the importance of GDPR and the protection of sensitive customer information Professional Requirements: - Have a more »

job description carefully before applying, thank you) Primary Objectives: The Quality Assurance Associate is responsible for helping to maintain and improve the DnaNudge Quality Management System as part of the Quality team by identifying potential improvements and efficiencies and helping to develop, revise and implement Quality procedures and policies. The … compliance of all regulatory requirements. Participate in the execution and support of internal and external regulatory audits and inspections. Support the maintenance of DnaNudge QMS program ensuring all processes are compliant to the relevant standards. · Manage some DnaNudge documentation associated with the QMS where required · Perform initial quality reviews of … internal auditor · (Desirable) Has worked in a similar role within the Medical Device/Pharmaceutical industry · (Desirable) Working knowledge and experience with a Quality Management System, such as deviations, investigations, CAPA, and customer complaints. · (Desirable) Experience of ISO certified QMS (ISO13485) Knowledge (Essential) In depth understanding of approaches to quality more »

AWE is currently recruiting for a Commissioning Engineer to provide due governance and management to meet specifications and acceptance criteria, within the QMS and Project Delivery processes and procedures, whilst organising and managing commissioning activities. Location : Reading area Package : £33,850 - c£44,000 (depending on your suitability and level more »

to the Clinical Development teams, providing guidance on GCP activities related to quality. Primary Responsibilities: Defining, maintaining, and monitoring the GxP Quality Management System (QMS). Making sure the QMS meets all the necessary regulatory requirements, with a strong focus on GCP compliance. Supporting and guiding the Clinical Development teams more »

operation, ensuring quality compliance throughout the business with focus on WDA, MIA and GMP and GDP activities. Key Responsibilities: To ensure that a quality management system is implemented and maintained and appropriate to the activities at the Company inclusive of the EU Guidelines on Good Distribution Practice of Medicinal Products … needed for successful site compliance to the PQS. Participating in reviews and suggesting improvements delving into areas of continuous growth. Responsible for updating & maintaining QMS related trackers. Ensure that the company operates in compliance with the authorised activities on the WDA and MIA licenses. Ensure that own premises and other more »

Job Summary QA Specialist is responsible for ensuring continued compliance of the Quality Management System of the company with the relevant Medical Device Directives, Medical Device Regulations, International Standards, and Customer Requirements and that this is maintained and implemented accordingly. Responsibilities Provide day-to-day support and be responsible to … maintain the effectiveness of the Quality Management System, including, but not limited to, Document Control, CAPA, Vigilance, Risk Management, Internal Audit, Post-Market Surveillance, Supplier Monitoring and Assessment and Product Release activities Contribute to strategic improvement projects to improve business processes in line with the applicable regulatory requirements and Medicareplus … times To show initiative in problem solving by identifying and recommending solutions to problems encountered To maintain a personal knowledge of the current Quality Management System and Regulatory Requirements Please note that the duties and responsibilities within this role may change over the course of employment, which will require flexibility. more »

Job summary This post is a Quality Assurance post specialising in Quality Management/GMP Documentation control and Quality Control. The post holder be part of the QA team, they will manage the Quality Management and Documentation control systems across more »

is responsible for managing all internal and external Quality Management aspects of a contract/project, ensuring implementation, maintenance, and improvement of the Quality Management System throughout the Tender, Project implementation, and After Sales support. Benefits: Remuneration: Competitive salary, an excellent package and hybrid working Professional Development: Opportunities for growth … equivalent qualification. Minimum 2 years of experience in a Quality Assurance role. Minimum 2 years of experience in customer-facing roles. Proficiency in quality management system requirements such as ISO9001/TL9000 (QMS). Desirable skills include Project Management, Basic Commercial Skills, and/or Lead Auditor training. How to more »

point of contact for their laboratories engaged in exploratory analysis of patient samples. You will be responsible for: Implementation of the company's quality management system relevant to GCP, including laboratory analysis of clinical samples, external vendor oversight, and training on quality procedures Acting liaison and support for Immunomonitoring and … assisting in quality assurance aspects of the company's Clinical Trials Act as the system administrator for the eQMS, write and/or review QMS documents, including SOPs, deliver training to laboratory teams and eQMS users Plan and conduct of audits, including internal, vendors, clinical sites, and external laboratories Provide more »

MEICA Project Manager We currently have a fantastic opportunity for an experienced MEICA Project Manager to join a career enhancing project in the West Midlands. Our client is working closely with Severn Trent Water on their Capital Delivery Framework, as more »

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 … system during regulatory and client audits/inspections. Management of the training matrix and Veeva Training to ensure fit for purpose. Provide support and QMS data for internal and external meetings, including the Quality/Metrics Strategic Working Group (SWG). Maintain reports and dashboards in Veeva. Provide eQMS training more »