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 QualityManagementSystem 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 ❯
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 QualityManagementSystem 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 QualityManagementSystem 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 ❯
Milton Keynes, Buckinghamshire, South East, United Kingdom
ARMS INNOVATIONS LIMITED
QualityManagementSystem (QMS), and exceptional people to deliver top-tier engineering and asset life-cycle management services in highly automated environments. Our Enterprise Level Software Platform and QualityManagementSystem offer real-time workflow automation, communication, and insights, ensuring safe and efficient operations that maximise business performance. Join us to be part of a team that is at the 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 qualitymanagementsystem (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 ❯
leads and maintains the departments software development programme and is responsible for providing policies and procedures pertaining to safe scientific computing practices within MPCE. The group leads the qualitymanagementsystem implementation programme and provides support and training to MPCE. The group provides qualitymanagement policies and procedures to comply with the relevant statutory and certification requirements, managing risks, incidents … with services supporting the operational management of the Medical Physics & Clinical Engineering department.1.4 To support the departmental audit activities.1.5 To assist with the operation and management of the qualitymanagementsystem in line with departmental policies and procedures1.6 To assist with the delivery of the personal dosimetry service1.7 To assist with the delivery of the radioisotope ordering service1.8 To support More ❯