continuous improvement efforts for vision systems, ensuring optimal performance and minimal downtime. Analyse inspection system data, monitor KPIs, and proactively drive improvements in accuracy and efficiency. Document system requirements, validation protocols, and compliance measures in line with medical device regulations. What You'll Need HNC, HND, or Degree in an Engineering or Scientific discipline. Hands-on experience integrating vision systems More ❯
addition, this role will take leadership responsibility of a small team across both shift and core days patterns. The key responsibilities in this role are: Overseeing the processing of validation and development lots through the manufacturing area in alignment with established plans/protocols Investigate, document and remediate Quality issues that arise; communicate and escalate as required Deliver the quality More ❯
activities. Participate in clinical study teams and liaise with other departmental groups to establish priorities and communicate schedules. Support clinical studies, including CRF design/review, database build and validation, creation of data management documents, and laptop setups. Manage and contribute to the monitoring of tasks and metrics to ensure quality and provide reports on project/task status. Establish More ❯
