Biomedical Scientist - Haemostasis
| Dyddiad hysbysebu: | 22 Medi 2025 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Negotiable |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 05 Hydref 2025 |
| Lleoliad: | London, W1T 4EU |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | E0111-25-0057 |
Crynodeb
Overall Job Purpose: To assist with the daily running of the laboratory section to which you have been assigned within the Department of Haemostasis. To assist in the performance of the routine diagnostic analytical work of the department as directed. To maintain the highest professional and technical standards in the department. Main duties To include but not be restricted to: Technical 1) To maintain technical competence in Haemostasis. 2) To handle, use and dispose of blood (and other body fluids or tissues) and hazardous chemicals in a safe manner. 3) To assist in the care and maintenance of equipment and to ensure equipment is functioning correctly, prior to analysis. 4) To carry out first line equipment and method troubleshooting, advise senior Biomedical Scientist of situations requiring further action, work with Service Engineers on fault resolution. 5) To prepare, store and use reagents required for laboratory investigations. 6) To perform manual, semi-automated and fully-automated laboratory investigations. 7) To measure and monitor the accuracy and imprecision of laboratory investigations using appropriate quality controls procedures. 8) To undertake preliminary fault finding and corrective action when the quality control procedures indicate loss of performance. 9) To report to the senior Biomedical Scientist any instance or event which may cause a service delivery failure. Scientific 1) To undertake method and laboratory instrument evaluation as directed by the Laboratory Operations Manager. 2) To participate in research and development as directed by the Laboratory Operations Manager. Diagnostic 3) To interpret first line laboratory results and take appropriate actions in line with: i. Laboratory policies and procedures for authorising results, adding approved. ii. Predefined clinically relevant comments, referring results for an expert opinion. iii. Clinical interpretation. 4) To report results through the laboratory computer system or by telephone to medical and nursing staff when requested to do so. 5) To inform the requestor of clinically significant results. 6) To provide approved departmental information and advice to other healthcare professionals and patients and to refer on to appropriate specialists requests for information out of their area of responsibility. 7) To participate in clinical audits Training and Education 1. To be competent in the area of work for which you have supervisory responsibility. 2. To make sure that training documentation is up to date and complies with UKAS, HCPC and IBMS regulations. 3. To further be actively involved in staff meetings and seminars. 4. To maintain own personal development and attend departmental meetings as required. 5. To maintain registration with the Health and Care Professions Council (HCPC) and participate in a recognised CDP scheme. 6. To take an active interest and keep abreast of developments in the discipline. 7. To assist in the development of junior colleagues by assisting in the training of trainee BMS and MLA staff, and to undertake, complete and sign off all competencies associated with these grades. 8. To undertake mandatory training as per HSL requirements.