Job summary
An exciting opportunity
has arisen at The Christie Pathology Partnership (CPP) for a suitably qualified
and experienced Specialist Biomedical Scientist to join our Blood Transfusion
department based in Manchester.
The Christie Pathology Partnership
was formed in 2014 and is a joint venture between The Christie NHS Foundation
Trust and SYNLAB, the largest provider of laboratory pathology and diagnostic
services in Europe. We provide Pathology
services for The Christie, which is the largest single cancer centre site in
Europe and the first UK centre to be accredited as a comprehensive cancer
centre. The Christie treats more than
60,000 patients a year.
CPP is based on-site at the
Christie Hospital which as a specialist site has no A&E or maternity
departments. The Blood Transfusion Laboratory is responsible for issuing
approximately 1000 red cell units and 400 platelets per month. The department is
a high user of all blood components due to the nature of the patients and
specialist theatre cases. Our transfusion laboratory is equipped with 2 x
Bio-Rad IH500 analysers, Contronics alarm system and Technidata LIMS. The
repertoire is automated group and screen, manual crossmatching, electronic
issue and antibody investigation. There is a large haematology and
transplantation unit, and you will work closely with the stem cell team to
support their activity.
Main duties of the job
The role will involve core
laboratory hours of Monday to Friday 08:30 - 17:00 with no requirement for
shift work. You will require specialised
knowledge and experience of laboratory techniques, analyser platforms and
associated equipment. As a specialist you will independently be able to advise and
identify atypical blood group antibodies. The role will require you to work
closely with the blood transfusion senior and support them with the day-to-day
running of the Blood Transfusion section ensuring UKAS and BSQR compliance.
This will include helping to train new members of staff and assess annual
competencies. Involvement in some quality management including auditing and
document review. You will need to be conversant with the main laboratory
information management system and middle-ware applications.
At SYNLAB, we believe in nurturing a culture of well-being and ensuring our employees are supported both professionally and personally. That's why we're thrilled to offer an exhilarating rewards package, including our incredible Wellbeing Allowance worth up to £1500 per annum for our esteemed team members working in Band 2 - 8 roles.
About us
SYNLAB UK & Ireland work closely with clinicians,
hospitals, occupational health providers and clinical researchers to provide a complete
pathology offering.
We operate in increasingly diverse environments which is
reflected in our workforce, clients, customers, suppliers, communities and
partners. We believe an inclusive workplace culture is the best way to source,
attract and retain diverse and talented people, and create a sustainable,
high-performing workforce.
We believe our staff is vital to the principle of making a
positive difference to healthcare, therefore, we promote a culture of
continuous personal development where scientists and staff have the support and
resources to acquire new skills and build their careers through learning and
development opportunities, coaching and clear career pathways.
We promote an open and collaborative culture where leaders
act as role models and facilitate a two-way communication, engage with staff
and stakeholders transparently and actively encourage feedback and suggestions.
We reserve the right to close any
adverts once we have received a sufficient number of applications. If you
decide to apply for this post but do not hear back from us within two weeks of
your application, please assume that you have not been short-listed on this
occasion.
SYNLAB UK & Ireland is a committed equal
opportunities employer and does not unlawfully discriminate on the basis of any
status or condition protected by applicable UK employment law.
Job description
Job responsibilities
Participate
in and assist with clinical trials, the development of new tests and research
& validation of equipment ensuring at all times compliance with all
policies as required by regulatory directives, accreditation bodies and local
management policies and practices.
To
provide technical advice to clinical staff
To
perform and interpret routine and specialist Biomedical investigations and to
participate daily in the scientific and technical activities of the laboratory
section under the supervision of senior staff.
Together
with Senior staff help ensure compliance with all policies as required by
regulatory directives, accreditation bodies and local management, including;
United
Kingdom Accreditation Services (UKAS)
Christie
Pathology Partnership policies and SOPs
MHRA
NHSCSP
HTA
HFEA
Any
other body in area of responsibility
Utilise
the laboratory LIMS, Q-Pulse quality monitoring system and other application
software according to authorised protocols including assisting in computer data
entry in all areas of the laboratory, document review, non conformance review
and quality assurance processes.
Communicate
efficiently, courteously and with clarity at all times, whether face to face,
telephone or electronic methods referring enquiries to senior staff where
appropriate. Matters being communicated
may include complex information and/or results.
Attend
and participate positively in laboratory and other meetings as directed by
Laboratory senior staff
As
directed by senior laboratory staff, plan and prioritise work allocations,
training plans, audits of both yourself and junior staff, responding
appropriately to the needs of routine and urgent activities.
Encourage
active participation in continuous professional development and support the
introduction of new technologies and / or systems by being a change advocate.
Report
all incidents and adverse events to senior staff and enter the information into
Datix in a timely manner.
Demonstrate on going competency against
training plans and participate
positively in CPD (continuous professional development) activities.
Safety:
To observe safety regulations and
attend mandatory fire, manual handling and other course as required.
To assist in the investigations
of any incidents.
Participate in risk assessment
monitoring
To ensure that the equipment
within area of work is maintained and operated as per SOPs
To comply with The Christie policy for annual mandatory updates and have
knowledge of COSHH and Lifting and Handling Policies
Job description
Job responsibilities
Participate
in and assist with clinical trials, the development of new tests and research
& validation of equipment ensuring at all times compliance with all
policies as required by regulatory directives, accreditation bodies and local
management policies and practices.
To
provide technical advice to clinical staff
To
perform and interpret routine and specialist Biomedical investigations and to
participate daily in the scientific and technical activities of the laboratory
section under the supervision of senior staff.
Together
with Senior staff help ensure compliance with all policies as required by
regulatory directives, accreditation bodies and local management, including;
United
Kingdom Accreditation Services (UKAS)
Christie
Pathology Partnership policies and SOPs
MHRA
NHSCSP
HTA
HFEA
Any
other body in area of responsibility
Utilise
the laboratory LIMS, Q-Pulse quality monitoring system and other application
software according to authorised protocols including assisting in computer data
entry in all areas of the laboratory, document review, non conformance review
and quality assurance processes.
Communicate
efficiently, courteously and with clarity at all times, whether face to face,
telephone or electronic methods referring enquiries to senior staff where
appropriate. Matters being communicated
may include complex information and/or results.
Attend
and participate positively in laboratory and other meetings as directed by
Laboratory senior staff
As
directed by senior laboratory staff, plan and prioritise work allocations,
training plans, audits of both yourself and junior staff, responding
appropriately to the needs of routine and urgent activities.
Encourage
active participation in continuous professional development and support the
introduction of new technologies and / or systems by being a change advocate.
Report
all incidents and adverse events to senior staff and enter the information into
Datix in a timely manner.
Demonstrate on going competency against
training plans and participate
positively in CPD (continuous professional development) activities.
Safety:
To observe safety regulations and
attend mandatory fire, manual handling and other course as required.
To assist in the investigations
of any incidents.
Participate in risk assessment
monitoring
To ensure that the equipment
within area of work is maintained and operated as per SOPs
To comply with The Christie policy for annual mandatory updates and have
knowledge of COSHH and Lifting and Handling Policies
Person Specification
Experience
Essential
- Competency to perform testing and validate results within Blood transfusion duties to defined protocols
- Ability to prioritise the workload according to clinical need, being able to multitask to maximise work output and to direct staff as required.
- Have knowledge of the operation and basic troubleshooting skills of blood group analysers.
- High knowledge of the statutory requirements for handling and storage of blood and blood products.
- Have good interpersonal skills, being able to communicate effectively to other professionals and patients.
- Competency to perform audits and understanding of quality management.
Qualifications
Essential
- HCPC registered as a Biomedical Scientist
- IBMS Specialist Diploma in Haematology with Hospital Transfusion Practice, or in Transfusion only with separate BBTS certificate, or equivalent specialist qualifications
Person Specification
Experience
Essential
- Competency to perform testing and validate results within Blood transfusion duties to defined protocols
- Ability to prioritise the workload according to clinical need, being able to multitask to maximise work output and to direct staff as required.
- Have knowledge of the operation and basic troubleshooting skills of blood group analysers.
- High knowledge of the statutory requirements for handling and storage of blood and blood products.
- Have good interpersonal skills, being able to communicate effectively to other professionals and patients.
- Competency to perform audits and understanding of quality management.
Qualifications
Essential
- HCPC registered as a Biomedical Scientist
- IBMS Specialist Diploma in Haematology with Hospital Transfusion Practice, or in Transfusion only with separate BBTS certificate, or equivalent specialist qualifications
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).
Additional information
Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.
UK Registration
Applicants must have current UK professional registration. For further information please see
NHS Careers website (opens in a new window).