Specialist Biomedical Scientist
| Dyddiad hysbysebu: | 27 Ionawr 2026 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Negotiable |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 08 Chwefror 2026 |
| Lleoliad: | London, SE1 8NZ |
| Cwmni: | NHS Jobs |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | U9206-26-0007 |
Crynodeb
This role supports the delivery of biomedical investigations as part of the laboratory in Synnovis. Reporting to the Operations Managers, you will hold a variety of responsibilities to ensure the successful delivery of pathology services, in line with our corporate objectives. You will hold a variety of accountabilities in the laboratory environment. These may include, but are not limited to: Perform and interpret routine and specialist biomedical investigations by participating in regular daily workloads, as directed by management, in line with your skills, experience and competencies. Maintain standards of conduct required by the HCPC to practice as a registered Biomedical Scientist. Provide technical advice to clinical colleagues as required and within limits of competency. Process specimens and handle sensitive information with care and due diligence, such as patient results, in line with local SOPs. Propose and implement changes to SOPs, policies and work practice as required. Participate in development of new tests, as directed, including alignment with accreditation bodies and local management processes. Where necessary this will include analysing clinical trial samples. Participate in verification and validation work when required. Day to day supervision of MLAs, APs and BMSs, providing support, training and mentoring to ensure performance is in line with laboratory standards. Observe all safety regulations and ensure others are doing the same. This includes holding people to account when standards fall short of expectations and raising concerns about safety in the laboratory. Ensure compliance for your area of work with all legislative and quality requirements of regulatory directives, accreditation bodies, and local management including: Care Quality Commission UKAS Synnovis policies and SOPs Any other body in area of responsibility. Participate in quality management activities including inspections, audits, EQA and IQC procedures as required. Utilise the Laboratory Information Management System (LIMS), Q-Pulse quality management database and other relevant software to ensure high quality reliable data capture and entry. Complete data entry accurately to record sensitive patient information, requiring frequent, long period of concentration whilst maintaining patient confidentiality and following Information Governance (IG) guidelines. Work closely with colleagues in the quality team to identify best practice and embed a culture of high quality and performance across your area. Report all incidents and adverse events to management and enter the information in the CAPA module of Q-pulse in a timely manner as directed, supervising and assisting junior colleagues with the process. Demonstrate ongoing laboratory-based competency against training plans. Demonstrate professionalism, patience and empathy when explaining complex subjects, and in particular when communicating with people who do not share same level of knowledge or understanding. Prioritise your workload effectively to ensure that deadlines are met, and that work is delivered to the highest standards possible. Take part in CPD activities to ensure that your practices and knowledge are always relevant and up to date to your specific area.