At Lancet Laboratories we recognise that results are achieved through attracting, developing and retaining delivery and collection of specimens from outlying laboratories, supporting doctors and clients to ensure that management and ensure safe working conditions as per Quality Assurance Standards. Minimum Criteria Required:
At Lancet Laboratories we recognise that results are achieved through attracting, developing and retaining delivery and collection of specimens from outlying laboratories, supporting doctors and clients to ensure that management and ensure safe working conditions as per Quality Assurance Standards. Minimum Criteria Required:
processes, participant recruitment, quality assurance, and laboratory/pharmacy tasks. Facilitate participant and attend relevant training. Review and action laboratory results. Interpret ECGs, CXRs, etc. Address monitoring
processes, participant recruitment, quality assurance, and laboratory/pharmacy tasks. Facilitate participant and attend relevant training. Review and action laboratory results. Interpret ECGs, CXRs, etc. Address monitoring
continuously monitor production outputs, concentrate quality conformance and optimise process efficiencies in required. Ensure adherence to quality requirements by monitoring laboratory feedback and ensuring the required
continuously monitor production outputs, concentrate quality conformance and optimise process efficiencies in required. Ensure adherence to quality requirements by monitoring laboratory feedback and ensuring the required
and reporting on the effectiveness of the HPA quality management system at the site, including implementation practice system, the utilization of standard process control mechanisms, forms, checklists and report structures supervising the development of site specific quality management and quality inspection plans. Minimize and eliminate Generating and maintaining process control documentation as necessary, (e.g Quality Inspection Plans, (QIPs), site drawing control –registration of drawings, maintaining current revision status, controlled issue drawings
and reporting on the effectiveness of the HPA quality management system at the site, including implementation practice system, the utilization of standard process control mechanisms, forms, checklists and report structures supervising the development of site specific quality management and quality inspection plans. Minimize and eliminate Generating and maintaining process control documentation as necessary, (e.g Quality Inspection Plans, (QIPs), site drawing control –registration of drawings, maintaining current revision status, controlled issue drawings
Driver's License
Management: