1 to 25 of 46 QMS Jobs in England

pathways, and a commitment to continuous improvement in patient outcomes. Your new role As QA Compliance Manager, you'll lead a team responsible for maintaining and improving the Quality Management System in line with GMP, ISO, and regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer audits. You'll More ❯

improvement in product and service quality Contribute to Quality improvement initiatives Maintain an auditable training record Maintain the quality documentation system Support the implementation, execution, and maintenance of the QMS, including but not limited to: Risk Assessments Change Controls CAPAs Deviations Complaints Recalls What we're looking for Manufacturing experience required (open to industries) Strong understanding in ISO 9001/ More ❯

skills, looking to make a meaningful impact in a GMP-licensed facility. Key Responsibilities: Lead and manage a team of QA Officers to ensure product release meets GMP and QMS standards. Support the QA Manager with site inspections, internal audits, and external regulatory visits. Oversee documentation control, SOP reviews, and CAPA implementation. Drive continuous improvement initiatives and training programmes across More ❯

and processes to improve the company’s Health & Safety, Environment, Quality and corporate responsibility performance. Lead the continuous development, implementation, and maintenance of the ISO 9001 Quality Management System (QMS) to ensure compliance with international standards and internal quality requirements. Lead training programs to foster a culture of safety among all employees. Develop, implement, and maintain comprehensive HSE management systems. … and maintain all necessary documentation. Skills and Qualifications Degree in Occupational Health and Safety, Environmental Science, or related field is desirable. Experience of delivering ISO 9001 Quality Management System (QMS)/holds formal Quality qualifications Proven experience in HSE management within a manufacturing environment Strong knowledge of relevant health and safety legislation and best practices. Excellent communication and leadership skills More ❯

for a proactive and detail-driven Quality Assurance & Compliance Officer (ISO 9001) to support a leading manufacturing company in West Bromwich. This role is ideal for someone experienced in QMS documentation or quality administration who is ready to take ownership of internal audits and compliance processes click apply for full job details More ❯

Skills: Proven hands-on experience with Biovia OneLab configuration and deployment Strong knowledge of system integration , including APIs, middleware, and data exchange protocols Deep understanding of Quality Management Systems (QMS) and laboratory workflows Familiarity with GxP compliance , validation documentation , and audit processes Excellent problem-solving, communication, and documentation skills If you are interested or would like to know more, please More ❯

Skills: Proven hands-on experience with Biovia OneLab configuration and deployment Strong knowledge of system integration , including APIs, middleware, and data exchange protocols Deep understanding of Quality Management Systems (QMS) and laboratory workflows Familiarity with GxP compliance , validation documentation , and audit processes Excellent problem-solving, communication, and documentation skills If you are interested or would like to know more, please More ❯

Skills: Proven hands-on experience with Biovia OneLab configuration and deployment Strong knowledge of system integration , including APIs, middleware, and data exchange protocols Deep understanding of Quality Management Systems (QMS) and laboratory workflows Familiarity with GxP compliance , validation documentation , and audit processes Excellent problem-solving, communication, and documentation skills If you are interested or would like to know more, please 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 - To prepare for and contribute to external audits with Customers and regulatory bodies. - To schedule and manage product and process audits More ❯

actions and preventative measures. Perform in-depth checks of packing materials and finished products when requested by the QA team and produce detailed reports. Audit sections of the Quality Management System to ensure compliance, reporting any non-conformances. Person Specification: Ability to demonstrate company values: Respect, Aspire, Courage, One Team & Diversity. Strong planning and organisational skills. Excellent attention to detail. More ❯

Experience: Proven hands-on experience with Biovia OneLab configuration and deployment. Strong expertise in system integration, including APIs, middleware, and data exchange protocols. Deep understanding of Quality Management Systems (QMS) and laboratory workflows. Ability to effectively communicate and collaborate with both business stakeholders and technical teams. Familiarity with GxP, validation documentation, and compliance standards. Excellent problem-solving, documentation, and interpersonal More ❯

live contracts; includes appropriate and timely escalation Ensuring all project artefacts (both deliverable & non-deliverable) are appropriately controlled and produced to a high standard, in-line with Roke's QMS Work with the Account team to identify opportunities for expansion and deliver against these. Person Specification Education and Qualifications APMP or PMP Qualifications. Knowledge, Skills & Experience Excellent Stakeholder Management and More ❯

programme risks, escalating issues where necessary to MOD and internal leadership. Drive continuous improvement initiatives across the programme, leveraging lean methodologies and best practices. Ensure compliance with Expleo's QMS, MOD customer processes, and all relevant legal and regulatory requirements. Business Development and Bid Activities Support business development and bid activities, including requirements capture, scope definition, cost estimation, and scheduling More ❯

electronic products using specified equipment and test instructions Set up and calibrate test equipment as required Troubleshoot and fault-find on products Analyse test results in line with quality management system requirements Operate flying probe, ATE, and JTAG systems Contribute to process improvements and update procedures as needed Maintain accurate records including debug logs, test databases, and batch reports Follow More ❯

shared commitment to improving patient outcomes. About the Role We're hiring a QA Compliance Manager to lead a team focused on maintaining and enhancing the Quality Management System (QMS) in compliance with GMP, ISO 9001, ISO 13485, and other regulatory standards. Reporting to the Head of Quality, you'll oversee internal audits, batch record reviews, CAPA systems, and customer … control.This is a senior-level opportunity with potential Qualified Person (QP) sponsorship for the right candidate. Key Responsibilities: Lead and develop the QA Compliance team Maintain and improve the QMS in line with EU GMP and ISO standards Oversee internal audits, CAPA management, and batch documentation review Host customer audits and support regulatory inspections Drive continuous improvement and contribute to More ❯

of Work: Full-time, 40 hours per week, with occasional out-of-hours work required. Quality System Responsibilities Comply with the requirements of the company's ISO 9001 Quality Management System, as detailed on the company's shared drive. REF More ❯

of Work: Full-time, 40 hours per week, with occasional out-of-hours work required. Quality System Responsibilities Comply with the requirements of the company's ISO 9001 Quality Management System, as detailed on the company's shared drive. REF-224 118 JBRP1_UKTJ More ❯

HR Rev 05 Engineering/manufacturing qualifications (completed apprenticeship, HNC,HND, etc). CADMAN-B software experience Progress Plus MRP software experience Experience working within an ISO 9000 quality management system desirable SALARY & BENEFITS Up to £33k (DOE) Monday to Thursday 7am - 5pm Fridays off every week! Overtime on a Friday offered Please call Clare on 07799 886594 for more More ❯

and UK MDR frameworks. Work closely with the RAQA team on device classification, documentation, post-market surveillance, and incident reporting. Ensure contracts and business practices align with MDR and QMS requirements. Advise on SaMD, AI governance, and compliance in multi-jurisdictional contexts. Support regulatory submissions and interactions with notified bodies or authorities. 3. Commercial & Procurement Support Draft, review, and negotiate More ❯

processes and procedures. Apply Lean Manufacturing and Six Sigma principles to reduce waste and improve operations. Support the selection, configuration, and rollout of IT systems (ERP/MRP, MES, QMS, etc.). Coordinate with engineering, operations, and IT teams to align processes with business goals. Provide clear documentation, SOPs, and training to enable sustainable adoption. Act as a bridge between More ❯

processes and procedures. Apply Lean Manufacturing and Six Sigma principles to reduce waste and improve operations. Support the selection, configuration, and rollout of IT systems (ERP/MRP, MES, QMS, etc.). Coordinate with engineering, operations, and IT teams to align processes with business goals. Provide clear documentation, SOPs, and training to enable sustainable adoption. Act as a bridge between More ❯

processes and procedures. Apply Lean Manufacturing and Six Sigma principles to reduce waste and improve operations. Support the selection, configuration, and rollout of IT systems (ERP/MRP, MES, QMS, etc.). Coordinate with engineering, operations, and IT teams to align processes with business goals. Provide clear documentation, SOPs, and training to enable sustainable adoption. Act as a bridge between More ❯

Mercurial. Ability to work independently, think creatively, and adapt to fluid requirements. Security clearance (or eligibility to obtain one). Nice to Have Skills: Experience in task leading, including QMS documentation and mentoring. Familiarity with Linux OS. Knowledge of avionics or mission systems domains. Proficiency in Jira for software task management. Understanding of Simulation Interoperability standards such as HLA, DIS More ❯

Mercurial. Ability to work independently, think creatively, and adapt to fluid requirements. Security clearance (or eligibility to obtain one). Nice to Have Skills: Experience in task leading, including QMS documentation and mentoring. Familiarity with Linux OS. Knowledge of avionics or mission systems domains. Proficiency in Jira for software task management. Understanding of Simulation Interoperability standards such as HLA, DIS More ❯

team Identify opportunities, solve problems, and drive continuous improvement across the EMEAA region. You ll ensure we meet and exceed ISO 9001:2015 standards, manage our Quality Management System (QMS), and collaborate across sites and brands to create a consistent, world-class approach to quality. This is a regional role with influence across multiple business units, requiring strong problem-solving … impact in a defined period. What you are already great at Lead Quality Governance: Ensure full alignment with ISO 9001:2015. Manage internal audits, facilitate management reviews, and maintain QMS integrity across sites. Standardise Across Brands: Foster Collaboration with cross functional teams to create a unified approach on processes and procedures. Embed Best Practices: Champion Six Sigma, PFMEA, and Control More ❯