Specialist Biomedical Scientist
- Complete routine and complex specialist biomedical investigations in accordance with standard operating procedures (SOPs) and within specific turnaround times.
- Deliver work autonomously within all regulations and legislative requirements.
- Operate and maintain complex laboratory equipment within all safety standards relevant to your area, including troubleshooting.
- Supervise and guide colleagues and answer questions as required.
- Use cost effective methods in your practice and maintain levels of consumable goods and supplies in your area, and report shortages accordingly.
- 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.
- BSc (Hons) IBMS accredited degree or equivalent
- HCPC State registration as a Biomedical Scientist
- Specialist portfolio in relevant discipline (if HCPC Registration via IBMS Portfolio route) or equivalent experience or FIBMS
- Evidence of ongoing Continuous Professional Development (CPD)
- Willing to work towards higher levels of education
- IBMS membership
- Significant demonstrable broad-based discipline specific practical experience
- Analysing, interpreting and technical validation of routine, complex and specialist results
- Using Laboratory Information Systems
- Development of special interest and expertise in one or more areas of the laboratory, for example Quality, Health & Safety, Training or IT
- Demonstrates a sound understanding of the physiology, pathology, and scientific principles relevant to specialism
- Demonstrates a high degree of skill and knowledge where interpretation of results can be highly subjective
- Well-developed physical skills, demonstrable ability to use precision equipment and consumables
- Leadership qualities with experience of coaching, coordinating and supervising a team
- Ability to troubleshoot highly technical and precision equipment
- Ability to troubleshoot problems arising on analytical platforms, manual assays and semi-automated procedures, and know when to escalate
- Competent at communicating verbally and in writing with colleagues and clinical staff
- Ability to effectively manage own time, able to prioritise work for self and others and able to plan activities within area of work
- Ability to maintain focus and concentration for extended periods of time
- Demonstrable knowledge and application of quality systems, with reference to ISO/UKAS
- Demonstrable knowledge and application of health and safety legislation and procedure
- Leadership qualities with experience of coaching, coordinating and supervising a team
- Contributory pension scheme
- Generous annual leave entitlement
- Ground breaking development
opportunities
- Job Description (PDF, 488.3KB)
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