Senior Biomedical Scientist - Diagnostic Cytology
| Dyddiad hysbysebu: | 10 Mawrth 2026 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Negotiable |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 15 Mawrth 2026 |
| Lleoliad: | London, W1T 4EU |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | E0111-26-0005 |
Crynodeb
Main duties 1. To provide a consistently efficient, accurate and world-class service to our clients and patients. 2. To produce high quality work and gain a deep understanding of the techniques employed in the department. 3. To participate in all areas of the service 4. To lead or assist in special laboratory service development projects as required. 5. To manage and be responsible for the day-to-day running of laboratory sub-sections as required. 6. To assist in specialised method development and validation as required. 7. To operate and maintain laboratory equipment according to departmental and manufacturers protocols and procedures. 8. To be familiar with and proficient in the use of the information technology systems within the department. 9. To participate in meetings and contribute to effective communication within the department. 10. To assist in planning ones own work and that of other staff within a section. 11. To be involved in staff recruitment and to conduct appraisals as required. 12. To demonstrate commitment to flexible working patterns, to meet the needs of the service. 13. Attend off-site clinics to support with sample preparation, staining and microscopy examination. Quality Representative A Quality Representative is defined as a responsible person within a department, and or site, who has day to day duties assigned to them that ensure the smooth running and appropriate monitoring of compliance on behalf of the department. The Quality Representative role has strong links with our centralised Quality Management Group (QMG) function within Sonic HealthCare UK. Liaising with the QMG Department to ensure the prompt communication, raising and documenting of incidents, including the identification of tasks and ensuring their timely closure. These duties include, but are not restricted to the following: Meeting Attendance o Attend scheduled Quality meetings chaired by the Quality Manager. Documentation Requirements o Monitor Q-Pulse acknowledgment of documents. o Reviewing procedures, ensuring controlled documentation is in place and in use Incidents, Complaints and Non conformities o Raise incidents /complaints on Q-Pulse & Datix. o Investigation of incidents o Review and monitor incident action target dates and follow up with owners to complete. o Monitor completion of incident investigations and chase overdue stages. Q-Pulse Change Controls o Review and monitor Change Control action target dates and follow up with owners to complete. Evaluation and Audits o Conducting Audits o Review CAPA action target dates and follow up with owners to complete. Equipmento Check completion of all equipment logs o EQA and IQC month reviews Reagents and Consumables o Review maintenance of the reagent inventory. o Review documentation of batch numbers, in-use and expiry dates. Training and Education 1. To maintain own personal development, keeping abreast of developments in the field and attend external, departmental meetings and personal training events as required. 2. To maintain registration with the Health and Care Professions Council HCPC, and participate in a recognised CPD scheme. 3. To take an active interest in and keep abreast of developments in the discipline. 4. To become a role model for and to further develop junior colleagues by assisting in the training of staff at all levels. 5. To undertake teaching, competency and induction of new staff in conjunction with the other senior staff, and be actively involved in staff meetings and seminars.