15 of 15 QMS Jobs in the South East

precise specification requirements. Provide hands-on manufacturing support, including basic mechanical assembly, component installation, and production assistance. Complete test reports and documentation in line with customer requirements and Quality Management System standards. Carry out product upgrades and modifications to assemblies and finished products. Interpret and implement engineering changes from documentation. Identify product quality or performance issues and raise non-conformances More ❯

PPE, equipment and stock levels within the vehicle. Report any damage or shortages to the office to enable replacements to be arranged as necessary. Be aware of the Quality Management System which includes policies in place to support the business and its aims including but not limited to Health & Safety, Environmental, Data Protection, Anti-bribery & equality. Further information can be More ❯

PPE, equipment and stock levels within the vehicle. Report any damage or shortages to the office to enable replacements to be arranged as necessary. Be aware of the Quality Management System which includes policies in place to support the business and its aims including but not limited to Health & Safety, Environmental, Data Protection, Anti-bribery & equality. Further information can be More ❯

finding and innovative solutions Ensure you are familiar with the department's output production targets Complete all necessary paperwork and update databases to meet the requirements of the quality management system Ensure compliance with all associated procedures applicable to the manufacturing process Maintain the highest level of workmanship and product standards, and ensure no scrap is created with minimal re More ❯

SaaS agreements. Operational & Structural Projects: Manage carve-out operations, including partial asset transfers and establishing subsidiaries in foreign jurisdictions. Develop and implement business continuity plans and Quality Management Systems (QMS). Risk & Incident Management: Devise and monitor risk mitigation strategies. Track and address quality-related incidents to maintain high standards. Influence & Lobbying: Define and execute strategies for industry influence and More ❯

SaaS agreements. Operational & Structural Projects: Manage carve-out operations, including partial asset transfers and establishing subsidiaries in foreign jurisdictions. Develop and implement business continuity plans and Quality Management Systems (QMS). Risk & Incident Management: Devise and monitor risk mitigation strategies. Track and address quality-related incidents to maintain high standards. Influence & Lobbying: Define and execute strategies for industry influence and More ❯

SaaS agreements. Operational & Structural Projects: Manage carve-out operations, including partial asset transfers and establishing subsidiaries in foreign jurisdictions. Develop and implement business continuity plans and Quality Management Systems (QMS). Risk & Incident Management: Devise and monitor risk mitigation strategies. Track and address quality-related incidents to maintain high standards. Influence & Lobbying: Define and execute strategies for industry influence and More ❯

involves working with suppliers, other organisations (e.g., for power supplies or regulations), and internal teams like Acquisition and Build. Youll ensure designs meet safety standards, capture planning requirements, support QMS processes, and chair client meetings on design matters. Whats in it for you? We offer a range of benefits designed to support your life in and out of work, some More ❯

QA Engineer, you will be at the forefront of our quality transformation, utilising data-driven insights to recognise opportunities and solve problems. You will oversee our Quality Management System (QMS) and ensure compliance with ISO 9001:2015 standards, while forging partnerships across multiple sites and brands to create a world-class quality approach. With your strategic mindset and strong problem More ❯

QA Engineer, you will be at the forefront of our quality transformation, utilising data-driven insights to recognise opportunities and solve problems. You will oversee our Quality Management System (QMS) and ensure compliance with ISO 9001:2015 standards, while forging partnerships across multiple sites and brands to create a world-class quality approach. With your strategic mindset and strong problem More ❯

an established pharmaceutical manufacturing company who are looking to recruit for an experienced QA Manager who will play a key role in the furthered development of the QA team, QMS, growth of department and recruitment planning; this is a great time to join a company very much on the up! The Role:- Directly managing a team of quality professionals, conducting … for all direct reports. Recruiting and onboarding of new staff members. Setting objectives for the team and providing regular feedback (and coaching). Developing, implementing and maintaining a comprehensive QMS suitable for both pharmaceutical and food/ingredients products. Championing improvements through risk management & route-cause analysis. Responsible for the functioning of the QMS, providing oversight to key stakeholders alike More ❯

responsibilities. Support CAMO Assurance and Surveillance Quality Audits against the clients AMO, proposing, discussing and executing Corrective Actions Plans. Ensure the correct and proper use of the QMS (Quality Management System). Ensure that the Apache CAw Management Support Team remain MRP compliant and have a positive contribution to the Mil CAM's approvals. Attend relevant weekly Safety Meetings to More ❯

maintain excellence. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Oversee and manage a quality management system (QMS) that complies with ISO 13485 standards. Handle document control, change management, corrective actions, training records, audits, and supplier oversight. Lead internal and external audits, ensuring systems are always ready for … I-II, FDA registration, and 510(k) processes. Maintain technical files and coordinate cross-functional inputs to meet regulatory deadlines. Key Skills and Requirements: Experience managing ISO 13485-compliant QMS and leading audits. Familiarity with Software as a Medical Device (SaMD) is essential. Strong knowledge of UKCA, MHRA, FDA regulations, and cybersecurity standards such as DTAC, DSPT, DCB, and Cyber More ❯

maintain excellence. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Oversee and manage a quality management system (QMS) that complies with ISO 13485 standards. Handle document control, change management, corrective actions, training records, audits, and supplier oversight. Lead internal and external audits, ensuring systems are always ready for … I-II, FDA registration, and 510(k) processes. Maintain technical files and coordinate cross-functional inputs to meet regulatory deadlines. Key Skills and Requirements: Experience managing ISO 13485-compliant QMS and leading audits. Familiarity with Software as a Medical Device (SaMD) is essential. Strong knowledge of UKCA, MHRA, FDA regulations, and cybersecurity standards such as DTAC, DSPT, DCB, and Cyber More ❯

Its exciting times at Axis Electronics, as part of the international Cicor Group, we have ambitious growth plans over the next 5 years, recently acquiring 3 new sites in the UK which expands our opportunity for growth and your opportunity More ❯