1 to 25 of 101 QMS Jobs in England

conducting audits, managing non conformances and fostering a culture of quality within the organisation. Key Responsibilities: Lead and manage the Quality team. Develop, implement, and maintain Quality Management Systems (QMS) for substation design and installation projects. Ensure compliance with National Grid, IEC, BS EN, and ISO 9001 standards, as well as health, safety, and environmental regulations. Oversee quality assurance across More ❯

for quality management, quality assurance, and quality auditing tasks related to pharmaceutical products. Ensuring products are fit for purpose before release for use or commercial sale. Maintaining and improving QMS' performance by ensuring items such as deviations, CAPA and change control for which you are the owner are progressed in a compliant and timely manner and all other items are … a timely manner in line with company procedures. Participate and/or host internal and external audits inclusive of customer and regulatory audits. Competent to author and approve routine QMS activities. Performing Root Cause Analysis using problem solving tools such as Fishbone, 5 Whys etc. Authors, reviews, and approves Controlled Documents in accordance with procedures. Will support in delivering the … site GMP training as required. Will conduct the internal audit programme. Will support the maintenance of the site QMS and facilitate reporting of relevant KPIs within department and across site as required. Ensure customer or supplier complaints are satisfactorily investigated and communicated. The Person:- The ideal Candidate will hold a degree in a STEM related subject Experienced in batch review More ❯

matters. Assist with third-party and customer audits, including the implementation of corrective actions. Manage the internal audit programme, perform internal audits, and oversee corrective actions. Maintain the Quality Management System, including inspection and test data and quality records. Support resolution of customer complaints in collaboration with the Quality team. Create and maintain Quality Plans to ensure compliance with contract … technical drawings and specifications. Familiarity with Geometric Dimensioning & Tolerancing is a plus. Good understanding of manufacturing processes and quality control systems. Required Experience: Working knowledge of ISO 9001 Quality Management System standards and practices. Familiarity with mechanical inspection equipment; experience with CMM or FARO arm is a plus. Experience managing calibration systems and document control. Competence in developing and applying More ❯

the management of quality in one or more groups to ensure a high standard of management is adhered to and the implementation of and compliance with UKTL's Quality Management System Key responsibilities The local source and first point of contact for Quality Control/Assurance best practice working closely with the Group Leaders, Delivery Managers and the Quality Assurance … Team to ensure a regular review of Quality compliance to teams. Responsible for the Compliance Management System (CMS) data integrity and adherence with UKTL's quality management system (including review of procedures, measurement records and software validation and competence records and uncertainty budgets) and implementation of relevant change control processes. Responsible to perform first line checks including that document controls … includingrequirements analysis, design, development, documentation, testing, maintenance &support. Be familiar with the implementation of Findable, Accessible, Interoperable and Reusable (FAIR) principles of data management. Working within a rigorous Quality Management System Taking a leading role within a team on continuous improvement Experience of enforcing quality standards Strong influencing, communication and presentation skills Ability to manage own time and to work More ❯

Job Title: Senior QA Specialist Salary: £38,000 - £45,000 Location: Greater Manchester SRG is currently working exclusively with a highly successful & award winning, CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all More ❯

Salary Quality Assurance Engineer - London - up to £55,000 + Bonus + Ex. Benefits - Permanent Play a leading role in maintaining the Quality Management System (QMS) at the UK site, ensuring all processes are compliant, up to date, and clearly owned. It drives internal and external audits, and leads root cause investigations, supporting key initiatives including system recertification and management … reviews. Above all, it promotes a collaborative, proactive approach to continuous quality improvement. Responsibilities Lead the upkeep and development of the site's QMS in line with ISO9001/TL9000 Develop, manage and deliver the internal audit programme using a risk-based approach Facilitate and support external audits Lead RCA investigations using 8D, 5 Whys and Ishikawa methodologies Drive the … business through a major QMS recertification initiative Lead annual Management Reviews in collaboration with all Process Owners Track audit findings and lead weekly meetings to ensure timely resolution Manage controlled documents and ensure timely updates and reviews Requirements Solid experience in a Quality role within a multidisciplinary or regulated environment Strong understanding of ISO9001 and quality systems Excellent communication skills More ❯

teams to maintain the highest levels of product safety, airworthiness, reliability, and customer satisfaction. II. Essential Duties and Responsibilities 1. Quality in Operations • Ensure maintenance of Quality Management System (QMS) in accordance with AS9100 • Oversee quality assurance and quality control processes, including inspection, audits and corrective actions. • Lead and mentor a team of quality system manager, engineers and technicians to More ❯

engage inproject related meetings in order to identify and advise on any potential quality related issues and to ensure thatquality requirements and regulations are considered. Author and maintain quality management system documentation Produce and maintain Quality Management Plans for new and existing projects Support project non-conformance recovery and closure through defined QMS procedures. Facilitate root cause analysis and corrective More ❯

third party surveillance and customer audits, including corrective actions that arise. Manage the internal audit programme, perform internal audits and manage corrective actions that arise. Maintenance of the Quality Management System, including maintaining inspection and test data across local Quality system records. Assist the Quality Director and Quality Manager in resolving customer complaints. Produce Quality Plans to ensure compliance with … others. Ability to read technical drawings and specifications. Geometrical Dimensioning & Tolerancing knowledge is an advantage. Thorough knowledge of fundamental manufacturing processes and control systems. Experience required in: ISO9001 Quality Management System requirements and maintaining a QMS. Mechanical measuring and inspection equipment. CMM or FARO arm experience would be an advantage. Calibration systems and control. Documentation systems and control. Raising and More ❯

Your mission Purpose of Job Act as the QA Documentation Controller for the business, ensuring that files stored and archived both within the electronic Quality Management System (eQMS; MasterControl) and outside of the eQMS are maintained appropriately according to relevant procedures. Support validation of the MasterControl system to assure compliance across all sites; supporting project and upgrade re-qualification activities. … Batch Numbers. Hard Copy Document Retention and Archiving. Organise and manage QA Document Control visibility and activities. Author and maintain procedural documents related to management of documents within the QMS Maintain documentation held externally from the QMS, including document issue, return and archiving as required Support QMS projects, including partaking in computer system validation activities where required Develop and deliver … training related to the QMS and any other role related training as required Support Periodic System Reviews as required Provide Key Performance Indicator Reports for departments as required. Key Performance Indicators The MasterControl document control system is maintained in a validated state General MasterControl administrative tasks are completed contemporaneously e.g. users are provided with access when applicable, documents are reviewed More ❯

re growing fast and looking for mission-driven individuals ready to make an impact. Your new role As Quality Manager, you'll take ownership of the Quality Management System (QMS), ensuring full compliance with ISO 13485 and associated regulatory standards. You'll lead internal and external audits, drive CAPA implementation, manage documentation and validation processes, and promote continuous improvement across … time, office-based role (minimum 3 days per week on site) with occasional international travel. What you'll need to succeed Hands-on experience managing ISO 13485:2016 compliant QMS Strong knowledge of risk management (ISO 14971), GCLP, CAPA, and validation (IQ/OQ/PQ) Background in biotech, biomedical science, immunology, or similar Solid understanding of regulatory submissions and … you'll get in return Competitive salary based on experience Bonus scheme eligibility Career progression in a fast-paced, high-growth biotech environment Opportunity to shape and scale the QMS from within Exposure to groundbreaking science and multidisciplinary collaboration What you need to do now If you're interested in this role, click 'apply now' to forward an up-to More ❯

experience with deep understanding of GxP regulations, FDA 21 CFR Part 11 compliance, and validation methodologies •? Design and develop complex integration flows connecting S/4HANA with LIMS, MES, QMS, and regulatory reporting systems using REST, SOAP, OData, IDoc, RFC protocols •? Lead and mentor team of 6-10 integration developers while collaborating with functional consultants and business stakeholders •? Ensure regulatory More ❯

for purpose management system is in place covering, quality, safety, security, health and environmental issues. Facilitate the implementation of the QSSHE management system. Support the maintenance of the Quality Management System utilised within the office. Provide leadership to the SNS organisation on quality issues. Support SNS QSSHE Team in the delivery of day-to-day activities such as Total Risk More ❯

workshops, and various related meetings. Maintenance of the organisation's quality and service management documentation, including regular reviews and updates to policies, procedures and guideline documents. Maintenance of the QMS/SMS risk and action logs. Liaison with external and internal auditors, review and issue of audits reports, maintenance of audit findings logs and proactive follow up of open findings. More ❯

that arise; communicate and escalate as required Deliver the quality message around site through team training, presentations and tool box talks Support the monitoring and compliance of the Quality Management System as it applies to site Operations Plan, conduct and review inspections for all areas as per the inspection plan. Communicate findings and work with areas leads to implement corrective More ❯

Review and validate SAP design and configuration to align with financial governance standards and business objectives. IT Quality Management: Support the implementation and maintenance of IT Quality Management Systems (QMS), including documentation. Guide teams through IT Quality SDLC processes (e.g., CSV, IQ/OQ/PQ) for SAP Finance & Non Finance-related systems. Collaborate with GSK-aligned teams or clients More ❯

communication with internal employees, managers, and customers, as needed. Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. Support and comply with the company's Quality Management System policies and procedures. Maintain regular and reliable attendance. Ability to act with an inclusion mindset and model these behaviors for the organization. Ability to work on a mobile device More ❯

root cause analysis investigations for internal non-conformances. Support continuous improvement teams for quality improvement and waste reduction. Support the QC manager in ensuring standards defined within the quality management system are maintained and reflect the correct standards to match customer expectation. To highlight inconsistencies and errors within QC documentation and processes Ensure these are recorded in an appropriate manner More ❯

We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting More ❯

We are seeking a Quality Assurance Specialist to join a leading pharmaceutica logistics company. This role focuses on supporting the implementation and maintenance of the Quality Management System (QMS) in line with ISO 9001 and ISO 13485 standards, and ensuring compliance with EU GDP guidelines. Key Responsibilities: Maintaining and enhancing the QMS to meet regulatory, ISO, and client requirements. Supporting More ❯

at the forefront of a cutting-edge AI product that's revolutionising medical diagnostics and transforming patient care. Key Responsibilities Oversee and develop our medical device Quality Management System (QMS) and Information Security Management System (ISMS), ensuring compliance with ISO 13485, MDSAP, US FDA QSR, EU MDR and ISO 27001. Implement and secure certification for an Artificial Intelligence Management System … and/or equivalent CENELEC standard(s). Act as primary liaison for certification bodies and regulatory authorities during external audits and inspections. Oversee the drafting and updating of QMS, ISMS procedures, work instructions and forms; ensure effective document … control and distribution. Oversee CAPA and complaint investigations for our medical devices and ensure that activities are initiated, planned, executed and closed within defined timelines. Analyse trends from quality management system data, coordinate internal audits, recommend systemic improvements, and report to management on QMS & ISMS effectiveness. Lead our quality training program and mentor cross-functional teams on quality best practices More ❯

Regulatory Affairs Specialist to join their QA/RA team on a 12-month maternity cover contract. Key Responsibilities: Lead and support continuous improvements within the Quality Management System (QMS) Collaborate with all departments and external stakeholders to maintain regulatory compliance Provide QA/RA expertise throughout product development and change control processes Guide risk management and post-market surveillance … Review SOPs, software development documents, and regulatory submissions Deliver training to ensure quality and regulatory understanding across the business Perform internal and supplier audits and support external inspections Validate QMS-related software and manage eQMS platforms Assist in compiling and maintaining technical and regulatory documentation Benefits At Genedrive, youll be part of a passionate and expert team, making a tangible More ❯

internal processes and procedures and external customer and regulatory requirements.• Maintain a clean, organised and safe working environment and organise 5S initiatives. • To ensure adherence to the group Quality Management System and compliance to all Customer and regulatory requirements including EASA Part 21, EN 9100 and NADCAP. • To prepare for and contribute to external audits with Customers and regulatory bodies. More ❯

Internal Auditor & Quality Systems Manager Job Type: Part-Time, Hybrid - up to 30 hours a week (flexible with days/hours) Location: Flexible (Hybrid with regular office presence in Portsmouth) Hourly Rate: £15.00-£18.00 We are seeking a part-time More ❯

to identify areas for reliability and quality improvement; initiating and facilitating actions to implement improvements effectively using problem-solving techniques (8D, 5Why, etc.). Responsibility for the maintenance of QMS, ensuring compliance with all regulatory requirements and standards adopted by the company. Formulate, develop, and promote policies, processes, procedures, objectives, and measures for the continued operation of QMS (e.g., Quality … instructions for company processes and procedures. Organise and conduct internal and external audits to ensure adherence to regulations and standards. Collate and deliver performance data as part of the QMS review to senior management. Identify training needs and implement company-wide compliance training. Train and coach staff regarding quality and environment functions. Establish quality contracts with customers and suppliers. Act More ❯