8 of 8 Permanent QMS Jobs in the South West

Technical Files and Design History Files. You will be regularly present within the manufacturing environment, investigating issues at source and ensuring the Quality Management System supports safe, compliant and effective operations. What you'll need to succeed You will have: Previous Quality Engineering experience within medical devices or another highly ...

support and maintenance, translating business requirements into MOM capabilities. Integrating MES with OT systems (SCADA, WCS, automation, IoT) and IT systems (ERP, PLM, LIMS, QMS, WMS) for real-time data flow. Ensuring MES projects are delivered on time and in line with key milestones. Troubleshooting MES issues and driving continuous ...

environments, including SCADA, WCS, automation, and IoT systems. - Enable reliable data flow between MES and IT systems such as ERP, PLM, LIMS, QMS, and WMS. - Drive troubleshooting and continuous improvement by identifying MES-related issues and implementing fixes. - Maintain clear functional and technical documentation, including data workflow descriptions, while helping ...

internal needs Provide system-level guidance and technical advice to other departments Maintain the requirements baseline for each product Comply with the company Quality Management System Maintain and develop specialist technical knowledge to support projects Support process improvement within the systems team and related functions Essential Requirements Knowledge of systems ...

associated with Principal Engineer or Engineer responsibilities, with appropriate support provided where necessary. All employees are expected to comply with the organisation's Quality Management System and to actively contribute to a positive health, safety and environmental culture. Employees are expected to identify and report incidents, hazards, risks and opportunities ...

based in Gloucester, is looking to recruit an experienced Quality Engineer to join their manufacturing team and support the ongoing development of their Quality Management System in line with ISO 13485 and regulatory requirements. This is an excellent opportunity for someone with a strong background in manufacturing who enjoys working … lifecycle, from internal auditing and CAPA management to validation, supplier quality and continuous improvement. Key responsibilities include: Maintaining and improving the Quality Management System (QMS) Planning and conducting ISO 13485 internal audits and supporting external audits Managing CAPAs, non-conformances, root cause investigations and change control Supporting supplier quality, validation ...

minimised. Ensure for tasks that the correct equipment is used. To ensure that MOD Standing Orders, and The Company’s Quality Management System (QMS) procedures, are understood and implemented while conducting any work tasks. Responsible for identifying and challenging unsafe practices before reporting using relevant systems. Responsible for identifying ...

Collaborate effectively with engineers, electricians, and client stakeholders to deliver integrated solutions Ensure all software, documentation, and testing procedures comply with Quality Management System (QMS) and client requirements Essential Experience (proficiency in one or more) Siemens TIA Portal including Step 7 (S7-1200/S7-1500) and legacy support ...