Job summary
The Clinical Pathology Partnership (CPP) Blood Sciences Department, based on-site at The Christie Hospital, is seeking an experienced and motivated Specialist Biomedical Scientist to join our team. The Christie is a world-leading cancer treatment centre and a specialist site with no Accident & Emergency or Maternity services.
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 treat more than 60,000 patients a year.
This is an exciting opportunity to contribute to a busy, high-quality diagnostic service at one of the UKs most respected specialist hospitals. This is a full-time permanent role and you will be expected to participate 24/7 rota.
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.
Main duties of the job
Our Haematology Biochemistry laboratory processes approximately 720,000 samples per year and is equipped with Siemens Atellica and Advia analysers, Coagulation ACL Tops and manual assays/techniques supporting both a Core Biochemistry & Haematology Laboratory. Together, these laboratories deliver a comprehensive service including tumour marker monitoring for patients undergoing cancer treatment.
Responsibilities
- Perform and interpret complex analytical investigations within Blood Sciences.
- Provide specialist advice on troubleshooting analyser and assay issues.
- Undertake validation and verification of new methods and equipment.
- Participate in EQA (External Quality Assessment) interpretation and reporting.
- Contribute to training and supervision of less experienced staff.
- Engage actively in quality management, including internal audits and document review.
- Operate and maintain competence with the Laboratory Information Management System (LIMS) and associated middleware applications.
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
Qualifications
Essential
- HCPC registration as a Biomedical Scientist
- IBMS Specialist portfolio in Blood Sciences, Haematology or Clinical Biochemistry or equivalent specialist qualifications with proven experience at Band 6 level in Blood Sciences (appointment at Band 5 with automatic progression to Band 6 on completion may be considered).
Person Specification
Qualifications
Essential
- HCPC registration as a Biomedical Scientist
- IBMS Specialist portfolio in Blood Sciences, Haematology or Clinical Biochemistry or equivalent specialist qualifications with proven experience at Band 6 level in Blood Sciences (appointment at Band 5 with automatic progression to Band 6 on completion may be considered).
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).