5 of 5 QMS Jobs in Scotland

collaboration skills, including distributed teams Desirable: Experience with Bluetooth/BLE integrations Medical device or regulated environment experience Experience with ISO 13485 or similar QMS Knowledge of IEC 62304, ISO 13485, or other relevant standards I f you’re passionate about building high‐impact mobile applications and want to help ...

better decisions, improving efficiency, and enhancing patient safety. Role Overview Were seeking a Senior Quality Assurance Engineer to lead and support Quality Management System (QMS) performance across design, manufacturing, service, and compliance functions. This role is pivotal in ensuring our medical devices are safe, effective, and compliant with global standards. … objectives, systemic responsibilities, and customer requirements, as defined by Executive Management in the Spacelabs Quality Policy. As part of maintenance of the Spacelabs Quality Management System, Senior Quality Assurance Engineers shall partake in some or all of the following responsibilities: Ensure high quality of products and services, by implementing ...

CAPA activities, ensuring effective resolution and prevention of issues Conducting internal audits and supporting external regulatory inspections Maintaining and improving Quality Management System (QMS) processes and documentation What Were Looking For Degree in Engineering, Quality, or a related discipline Strong … experience in quality assurance within medical devices or regulated environments Proven background working with Design Controls and Risk Management Solid understanding of Quality Management Systems (QMS) Experience supporting new product development within regulated frameworks Knowledge of software within medical devices (SaMD) is highly desirable Strong communication skills with the ability ...

pivotal role in ensuring our medical devices are safe, effective, and compliant. This individual will lead Design Controls, Risk Management, and Quality Management System (QMS) governance throughout the product lifecycleprimarily focusing on design and pre-market activities. Acting as a trusted partner to R&D and Regulatory Affairs, you will … impact design decisions, safety, or documentation. Communicate trends or recurring issues to design teams. Support corrective actions or design improvements based on nonconformance insights. QMS Administration Conduct internal quality audits to verify compliance with procedures and regulatory expectations. Lead or support CAPA activities, ensuring effective verification and complete documentation. Manage ...

candidate information, maintaining digital records, and preparing training materials. Maintain digital filing systems and document control in line with the company Quality Management System (QMS) and data protection requirements. Assist with CRM updates, training orders, quotations, and job completion follow-ups using internal tracking systems and Excel logs. Support digital ...