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An established industry player is seeking an Advanced Biomedical Scientist in Clinical Immunology. This role is pivotal in managing laboratory operations, ensuring quality standards, and leading a dynamic team. The successful candidate will possess a strong background in biomedical science, with an MSc or equivalent qualification and HCPC registration. You will be responsible for delivering training, troubleshooting complex laboratory equipment, and maintaining UKAS accreditation. Join a forward-thinking organization that values collaboration, accountability, and empowerment, where your contributions will directly impact patient care and service quality.
Job summary
Expected Shortlisting Date
20/05/2025
Planned Interview Date
27/05/2025
Applications are invited for a HCPC Registered Advanced Biomedical Scientist in Clinical Immunology. Candidates will be well organised and able to manage and prioritise their workload successfully. Excellent communication skills are essential, as well as the ability to cultivate and maintain good working relationships with service users, colleagues and senior managers.
The successful candidate must have HCPC registration as a Biomedical Scientist and possess an MSc or equivalent postgraduate qualification in Biomedical Science. Experience of leading a team, quality management and/ or service improvement would be advantageous for this role.
We would invite applications from enthusiastic individuals who can demonstrate the confidence and capabilities required of this role.
For any queries please contact Chris Stageman - chris.stageman@nhs.net
Shortlisting date: 20 May 2025
Interview date: 27 May 2025
Main duties of the job
Our current instrumentation includes: Bioplex, Quantalyser slide processors, BNII nephelometers, Sebia Capillarys and Hydrasys electrophoresis systems, Phadia Immunocap 250, DS2 ELISA and Blot One.
You would be expected to have experience in delivering training, analyser troubleshooting and Quality management systems. You must have good knowledge of immunofluorescence slide interpretation, gel and capillary electrophoresis interpretation and a range of Immunology analytical instruments, be confident in leading a team and have good communication skills.
Main duties of the job
Quality activities to maintain UKAS accreditation status
Training and supervising of BMS and MLA staff and maintaining staff competency logs
Managing staffing in the section
Ensuring analysers are maintained correctly and undertaking any troubleshooting that is required; dealing with engineer visits for maintenance and repairs.
Organising the section around planned and unplanned analytical down time
Stock control and ordering of reagents and materials
Please read the attached job description and person specification for further details.
About us
The Immunology Department at Leeds Teaching Hospitals Trust is a regional, consultant led diagnostic and clinical immunology service. The diagnostic laboratory is currently based at the Old Medical School at Leeds General Infirmary and will be moving to our new purpose designed laboratory on the St James site in summer 2025. This move is in conjunction with the implementation of a new Managed Service Contract and a new LIMS.
THE LEEDS WAY VALUES
Our values are part of what make us different from other trusts, so we see this as a strength, as well as a responsibility. They have been developed by our staff and set out what they see as important to how we work. Our five values are:
Patient-centred
Collaborative
Fair
Accountable
Empowered
All our actions and endeavours will be guided and evaluated through these values
Leeds Teaching Hospitals is committed to our process of redeploying 'at risk' members of our existing workforce to new roles. As such, all our job adverts are subject to this policy and we reserve the right to close, delay or remove adverts while this process is completed. If you do experience a delay in the shortlisting stage of the recruitment cycle, please bear with us while this process is completed, and contact the named contact if you have any questions.
Job description
Job responsibilities
PRINCIPAL DUTIES & AREAS OF RESPONSIBILITY
In addition, computer skills are essential to carry out your work.
In order to work effectively in the role you as the job holder must be able to demonstrate a number of attributes and abilities. These will include:
Clinical/ Scientific /Technical (lab based roles)
Perform a wide range of complex clinical technical procedures. These will include the safe and effective use of highly complex laboratory equipment. Your level of knowledge and understanding of these procedures will be consistent with that to allow you to recognise system failures and errors. You will understand the need to report adverse events in the event of errors and failures.
Use of the LIMS to report, retrieve and manage technical information
To gain new knowledge through experience, formal study and participation in relevant training schemes
To be a leading member of a team providing a clinical technical service
To work independently when and as required by the service, for instance when working alone in the provision of the emergency on-call service.
To communicate, explain complex information and results to clinicians & other service users clearly and effectively whether orally, graphically or electronically
Oversight responsibility for co-ordinating effective workload management with prioritisation of samples received within specialist area
Responsible for the development and validation of in house quality control material & reagents
To validate the work of other sections when circumstances require
To work with precision and follow accurately the documented laboratory standard operating procedures
To operate highly complex laboratory equipment safely and efficiently
To input, manage, extract and interpret complex patient data using the laboratory computer system
To demonstrate relevant tasks to others as appropriate
To contribute actively towards the improvement of general service quality by participation in relevant discussions with other team members and leaders of other sections within the speciality
Attend MDT meetings as appropriate
Leadership and Management
Support the departments senior team and deputise in the absence of key staff to deliver service
To plan and implement changes to the clinical technical service offered by the section
To remain competent in established procedures and to develop new skills subject to the requirements of the service
Responsible for carrying out appraisal scheme for direct reports
Day to day management and responsibility for people governance procedures that are consistent with Trust HR policies for direct reports
To undertake tasks that contribute to the general management of the speciality
To take account of changes in service delivery by demonstrating a flexible approach to work
Effectively administers Trust people governance policies and procedures within area of specialist responsibility and undertakes the necessary training to ensure on-going competence delivery
Provides personalised support to promote the continuous development of staff as part of on-going line management responsibilities
Responsible for ensuring continuous individual and team development and a collaborative approach
Level 2 investigations
Roster approval level 1
Budgetary awareness for designated area and works with operational leads to maintain expenditure relating to area of specialist responsibility within agreed limits
Produces informative management reports and contributes to business cases which inform strategic decision making
Effective stock management
Quality / Training
Responsible for ensuring that quality management system and training documentation is up to date and fit for purpose at all times for area of specialist responsibility
Leads on the maintenance of a robust programme of training and competency assessment within the area of specialist responsibility, ensuring that procedures are only undertaken by staff with the requisite knowledge and skills at all times
Oversight of creation and authorisation of Standard Operating Procedures, risk assessments and training records within area of specialist responsibility
Have knowledge and understanding of current national legislation and guidelines relevant to the speciality
Ensures the maintenance of a safe working environment. This will include an awareness of the hazards associated with your work. In addition you will be aware of any suitable actions to take in the event of breaches in health and safety. Such hazards include fire, manual handling, breaches of security, controlled and uncontrolled exposure to chemical, biological and radioactive materials.
Ensuring that training and competency assessment take place at appropriate intervals and across all personnel, both on a scheduled and ad-hoc basis (e.g. in response to incidents)
Responsible for ensuring that quality assurance records are being consistently completed in a timely manner with documented assurance through audit
Responsible for ensuring that all audit nonconformities relating to the area of specialist responsibility are robustly investigated with timely instigation of remedial and corrective measures in order to successfully mitigate risk
Leads on service improvement initiatives for the area of specialist responsibility, empowering all staff to actively contribute to continuous improvement (e.g. establishment of standard work)
Leads on the implementation of new or updated technologies/instrumentation/tests within specialist area
Responsibility for the management of analytical result quality within area of specialist responsibility, including timely and effective review of EQA, IQC data, establishment and review of uncertainty, data trending, conducting quality investigations, implementing preventative, corrective and remedial follow up
Leads on service improvement initiatives for the area of specialist responsibility, empowering all staff to actively contribute to continuous improvement (e.g. establishment of standard work)
Actively contributes to service development within area of specialist responsibility by leading on the evaluation of new approaches to service delivery/updated technologies/instruments/ tests
Responsible for ensuring that appropriate service continuity plans and action cards are in place for area of specialist responsibility and subject to regular review of effectiveness
Maintain patient confidentiality. You will recognise the absolute requirement to protect sensitive information that is related to patient care.
Observe the requirements of departmental policies relating to service provision, for example sample labelling and adverse event reporting.
Observe the requirements of Trust policies relating to clinical and people governance.
Other
The principal duties listed above are not an exhaustive list and the post holder will be expected to undertake other duties as commensurate with the grade and role as as agreed with line manager. Addendums to this Job Description may be added to more accurately describe additional duties for non-lab based roles.
This job requires a high degree of dexterity and precision when manipulating small tools such as pipettes, handling very small volumes of clinical material or when preparing microscope slides for examination. Working with both speed and accuracy is required.
The post holder is responsible for maintaining their competency for all relevant technical and managerial/leadership elements of the role
Job description
Job responsibilities
PRINCIPAL DUTIES & AREAS OF RESPONSIBILITY
In addition, computer skills are essential to carry out your work.
In order to work effectively in the role you as the job holder must be able to demonstrate a number of attributes and abilities. These will include:
Clinical/ Scientific /Technical (lab based roles)
Perform a wide range of complex clinical technical procedures. These will include the safe and effective use of highly complex laboratory equipment. Your level of knowledge and understanding of these procedures will be consistent with that to allow you to recognise system failures and errors. You will understand the need to report adverse events in the event of errors and failures.
Use of the LIMS to report, retrieve and manage technical information
To gain new knowledge through experience, formal study and participation in relevant training schemes
To be a leading member of a team providing a clinical technical service
To work independently when and as required by the service, for instance when working alone in the provision of the emergency on-call service.
To communicate, explain complex information and results to clinicians & other service users clearly and effectively whether orally, graphically or electronically
Oversight responsibility for co-ordinating effective workload management with prioritisation of samples received within specialist area
Responsible for the development and validation of in house quality control material & reagents
To validate the work of other sections when circumstances require
To work with precision and follow accurately the documented laboratory standard operating procedures
To operate highly complex laboratory equipment safely and efficiently
To input, manage, extract and interpret complex patient data using the laboratory computer system
To demonstrate relevant tasks to others as appropriate
To contribute actively towards the improvement of general service quality by participation in relevant discussions with other team members and leaders of other sections within the speciality
Attend MDT meetings as appropriate
Leadership and Management
Support the departments senior team and deputise in the absence of key staff to deliver service
To plan and implement changes to the clinical technical service offered by the section
To remain competent in established procedures and to develop new skills subject to the requirements of the service
Responsible for carrying out appraisal scheme for direct reports
Day to day management and responsibility for people governance procedures that are consistent with Trust HR policies for direct reports
To undertake tasks that contribute to the general management of the speciality
To take account of changes in service delivery by demonstrating a flexible approach to work
Effectively administers Trust people governance policies and procedures within area of specialist responsibility and undertakes the necessary training to ensure on-going competence delivery
Provides personalised support to promote the continuous development of staff as part of on-going line management responsibilities
Responsible for ensuring continuous individual and team development and a collaborative approach
Level 2 investigations
Roster approval level 1
Budgetary awareness for designated area and works with operational leads to maintain expenditure relating to area of specialist responsibility within agreed limits
Produces informative management reports and contributes to business cases which inform strategic decision making
Effective stock management
Quality / Training
Responsible for ensuring that quality management system and training documentation is up to date and fit for purpose at all times for area of specialist responsibility
Leads on the maintenance of a robust programme of training and competency assessment within the area of specialist responsibility, ensuring that procedures are only undertaken by staff with the requisite knowledge and skills at all times
Oversight of creation and authorisation of Standard Operating Procedures, risk assessments and training records within area of specialist responsibility
Have knowledge and understanding of current national legislation and guidelines relevant to the speciality
Ensures the maintenance of a safe working environment. This will include an awareness of the hazards associated with your work. In addition you will be aware of any suitable actions to take in the event of breaches in health and safety. Such hazards include fire, manual handling, breaches of security, controlled and uncontrolled exposure to chemical, biological and radioactive materials.
Ensuring that training and competency assessment take place at appropriate intervals and across all personnel, both on a scheduled and ad-hoc basis (e.g. in response to incidents)
Responsible for ensuring that quality assurance records are being consistently completed in a timely manner with documented assurance through audit
Responsible for ensuring that all audit nonconformities relating to the area of specialist responsibility are robustly investigated with timely instigation of remedial and corrective measures in order to successfully mitigate risk
Leads on service improvement initiatives for the area of specialist responsibility, empowering all staff to actively contribute to continuous improvement (e.g. establishment of standard work)
Leads on the implementation of new or updated technologies/instrumentation/tests within specialist area
Responsibility for the management of analytical result quality within area of specialist responsibility, including timely and effective review of EQA, IQC data, establishment and review of uncertainty, data trending, conducting quality investigations, implementing preventative, corrective and remedial follow up
Leads on service improvement initiatives for the area of specialist responsibility, empowering all staff to actively contribute to continuous improvement (e.g. establishment of standard work)
Actively contributes to service development within area of specialist responsibility by leading on the evaluation of new approaches to service delivery/updated technologies/instruments/ tests
Responsible for ensuring that appropriate service continuity plans and action cards are in place for area of specialist responsibility and subject to regular review of effectiveness
Maintain patient confidentiality. You will recognise the absolute requirement to protect sensitive information that is related to patient care.
Observe the requirements of departmental policies relating to service provision, for example sample labelling and adverse event reporting.
Observe the requirements of Trust policies relating to clinical and people governance.
Other
The principal duties listed above are not an exhaustive list and the post holder will be expected to undertake other duties as commensurate with the grade and role as as agreed with line manager. Addendums to this Job Description may be added to more accurately describe additional duties for non-lab based roles.
This job requires a high degree of dexterity and precision when manipulating small tools such as pipettes, handling very small volumes of clinical material or when preparing microscope slides for examination. Working with both speed and accuracy is required.
The post holder is responsible for maintaining their competency for all relevant technical and managerial/leadership elements of the role
Person Specification
Skills & behaviours
Essential
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