Job summary
An exciting opportunity has arisen at The Christie Pathology Partnership (CPP) for a qualified and experienced Specialist Biomedical Scientist to join our Blood Sciences department.
We are looking for a keen, enthusiastic biomedical scientist with an interest in developing services to help us continue to deliver exceptional, high-quality integrated care to our patients. CPP is an excellent place to train and develop new skills and further study will be supported. This is a particularly interesting time to join CPP as plans are currently under discussion for the construction of an Advanced Pathology Centre at the Christie.
This is an excellent opportunity for a BMS to continue their professional development at one of the largest cancer centres in Europe.
Essentially, the role is to participate in the scientific work of the Blood Sciences department in line with the 24/7 shift rota.
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.
Main duties of the job
In this role, you will provide support across all areas of the laboratory as required, carrying out designated duties in line with local working practices while maintaining high professional standards and adhering to Health and Safety regulations. You will be responsible for performing and interpreting both routine and specialist biomedical investigations autonomously, ensuring patient results are delivered accurately and within agreed quality standards and turnaround times, under the supervision of senior staff. Working independently, you will also implement and propose improvements to procedures within your work area and may act as a lead specialist. Commitment to ongoing personal and professional development through academic study and practical experience is expected, alongside providing leadership, guidance, and training to Basic Grade staff, Trainee Biomedical Scientists, Associate Practitioners, and Medical Laboratory Assistants. As a registered Biomedical Scientist, you will be required to uphold the professional standards of conduct set by the Health Professions Council and provide specialist technical advice to clinicians regarding the appropriateness of tests and reporting timescales.
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
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) /Clinical Pathology Accreditation
(CPA)-Christie Pathology Partnership policies and SOPs-MHRA-NHSCSP-HTA-HFEAAny 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) /Clinical Pathology Accreditation
(CPA)-Christie Pathology Partnership policies and SOPs-MHRA-NHSCSP-HTA-HFEAAny 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 State Registration as a Biomedical Scientist in Blood Sciences discipline and evidence of CPD
- BSc (Hons) Biomedical degree or equivalent
- IBMS Specialist Portfolio or equivalent (required for Band 6)
- An advanced understanding of basic theoretical and practical Biomedical Sciences and technically adept at majority of routine and advanced laboratory procedures
Person Specification
Qualifications
Essential
- HCPC State Registration as a Biomedical Scientist in Blood Sciences discipline and evidence of CPD
- BSc (Hons) Biomedical degree or equivalent
- IBMS Specialist Portfolio or equivalent (required for Band 6)
- An advanced understanding of basic theoretical and practical Biomedical Sciences and technically adept at majority of routine and advanced laboratory procedures
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.