Principal Biomedical Scientist
| Dyddiad hysbysebu: | 01 Awst 2025 |
|---|---|
| Cyflog: | Heb ei nodi |
| Gwybodaeth ychwanegol am y cyflog: | Negotiable |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 17 Awst 2025 |
| Lleoliad: | London, SE1 8NZ |
| Cwmni: | NHS Jobs |
| Math o swydd: | Cytundeb |
| Cyfeirnod swydd: | U9206-25-0050 |
Crynodeb
At Synnovis, we are currently shaping the future of pathology services by creating a world-leading Hub and Spoke pathology network with our NHS partners. A large part of this modernisation will involve moving 70% of our services to a purpose built, state of the art Hub laboratory in the heart of London. The job you are applying for will be based at our Hub laboratory in Blackfriars, Southwark, SE1, however some work will remain in the refurbished essential services laboratories (ESLs) across our hospital network which includes The Royal Brompton and Harefield Trust, Guys and St. Thomas Hospital, Kings College Hospital at Denmark Hill and Kings College Hospital at The Princess Royal Hospital in Orpington, which will focusing on the rapid turnover of urgent tests. Please do ask your recruiting manager if you wish to find out more. Main Duties and Responsibilities of the role: You will hold a variety of accountabilities in the laboratory environment. These include, but are not limited to: Plan, organise and manage teams of Biomedical Scientists with a diverse range of skills, knowledge, and experience, performing biomedical analyses and processes on more than one site. Ensure a high-quality standard of service delivery, meeting key performance indicators. Provide professional leadership to Senior Specialist Biomedical Scientists, Specialist Biomedical Scientists, Biomedical Scientists, Trainee Biomedical Scientists, Associate Practitioners and Medical Laboratory Assistants. Provide an expert level of technical and operational knowledge to the laboratory services in Synnovis. This means being responsible for, and ensuring that, specialist training is delivered to scientific staff and support workers and other healthcare professionals. Provide expert technical advice and highly specialist information in your area of responsibility to clinical and other healthcare professions where patient care might be affected. Analyse samples in line with local practices including but not limited to recording results and necessary action on the Laboratory Information Management System (LIMS), ensuring all Information Governance (IG) requirements are met. Ensure all staff are following Standard Operating Procedures (SOPs) for safe use of laboratory equipment in accordance with manufactures guidance. Lead in the strategic development of the analytical service. Manage the introduction and implementation of new techniques, equipment and tests to realise patient and corporate benefits. Initiate and oversee the implementation of new techniques, equipment, and tests, as directed, including all verification and validation work. Where necessary this will include analysing clinical trial samples. Be responsible for the scientific overview of procurement of equipment and reagents within the laboratory. Participate in continuous service improvement initiatives. Provide expert technical advice and specialist scientific information to clinicians as to the appropriateness of tests, timescales and guidance as required. Be an ambassador for your area of expertise, presenting at conferences and seminars to share developments, innovations and training. Ensure all incidents and events are correctly reported by junior staff in Q-Pulse quality management data base and other relevant software and support them in learning quality procedures and investigations. In conjunction with the Quality team, supervise the monitoring, reporting and actions of errors, hazards, and incidents logged in the CAPA module of Q-Pulse. This may include taking part in investigations of incidents and providing expert insight into making improvements based on outcomes. Participate in appropriate clinical audits as required. Supervise and monitor, EQA and IQC reports and ensure any required corrective action is taken. Ensure compliance 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 Line manage employees, as required. This includes delivering all aspects of people management, such as recruitment, performance management, absence management, learning and development, employee health and wellbeing. Encourage junior employees in their scientific expertise, knowledge and professional development, including the safe use of highly complex and sensitive equipment. Review and authorise relevant documents, including SOPs, COSHH and risk assessments in line with the ISO 15189 standard. Ensure that all Synnovis policies and procedures are implemented and maintained and where necessary propose policy and service changes. Attend, and where required, chair regular departmental meetings and contribute to effective communication within the department. Deputise for the Operations Manager including attendance at meetings, as required. Take part in CPD activities to ensure that your practices and knowledge are always relevant and up to date to your specific area. Synnovis is a pathology partnership between SYNLAB UK and Ireland, and the NHS, including sites, Guys & St Thomas NHS Foundation Trust and Kings College Hospital NHS Foundation Trust, to deliver and transform pathology services across South East London. The partnership provides services to 1.7 million people living in South East London, as well as to hundreds of thousands of patients from outside the region who use local healthcare services. The partnership provides diagnostics, testing and digital pathology for hospital trusts, GP services and other healthcare providers.