Job summary
We
have an exciting opportunity for a HCPC Registered Biomedical Scientist with expertise
in Haematology to join our team on a fixed term basis. We are seeking
individuals who are dedicated to providing a high-quality patient centric
service and are enthusiastic about mentoring and sharing their knowledge.
Your
main site of work will be the SPS Hub laboratory working as part of a Blood
Sciences team of Biomedical Scientists to provide haematology test results for
patients in primary care across the county of Somerset as well as from both
Musgrove Park Hospital and Yeovil District Hospital.
SYNLAB UK & Ireland have established
experience of working in partnership with the NHS to deliver and improve
pathology services through its existing pathology joint ventures - including
Southwest Pathology Services (SPS).
Our team at SPS have been
fundamental to the principle of making a positive difference to healthcare in
Somerset for over a decade. We hold ISO15189 UKAS accreditation and are
an HCPC approved training Laboratory for both IBMS Registration and Specialist
Portfolios.
At SYNLAB, we believe in
nurturing a culture of well-being and ensuring our employees are supported both
professionally and personally. We offer a Wellbeing Allowance worth up to £1500
per annum for our esteemed team members working in Band 2 - 6 roles.
Main duties of the job
As a Biomedical
Scientist within the Blood Sciences team, you will perform and interpret
routine and specialist testing providing patient centred scientific excellence
whilst maintaining high quality standards in accordance with ISO15189.
You will
supervise, mentor and support other Biomedical Scientists, Trainee Biomedical
Scientists, Associate Practitioners and Medical Laboratory Assistants within
your department, sharing your knowledge, experience and passion for your work.
As a registered
Biomedical Scientist, you will have the responsibility of maintaining fitness
to practice and are required to participate actively in CPD. SPS will commit to support you in developing
your skills and knowledge in line with your professional growth and our
business interests. A dedicated Training team and extensive resources are
available to support this.
Most
importantly, through our shared values, you will help to make a positive
difference to the lives, health and wellbeing of those within our community
that we serve.
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 are 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 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; Clinical Pathology Accreditation (CPA), Southwest Pathology Service 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.
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.
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 iPP 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; Clinical Pathology Accreditation (CPA), Southwest Pathology Service 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.
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.
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 iPP policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies.
Person Specification
Experience
Essential
- A good understanding of the clinical significance of results and ability to interpret and act upon the results you are producing in a lone working setting
- Confident to make decisions in line with guidelines and written procedures to provide patient results including blood film morphology and special coagulation assays
Experience
Essential
- A good understanding of the clinical significance of results and ability to interpret and act upon the results you are producing in a lone working setting
- Confident to make decisions in line with guidelines and written procedures to provide patient results including blood film morphology and special coagulation assays
Experience
Essential
- A good understanding of the clinical significance of results and ability to interpret and act upon the results you are producing in a lone working setting
- Confident to make decisions in line with guidelines and written procedures to provide patient results including blood film morphology and special coagulation assays
Qualifications
Essential
- HCPC registration as a Biomedical Scientist with a Biomedical degree or equivalent and evidence of CPD, with post registration experience working in Haematology and proven ability to prioritise and manage own workload.
- To commence employment as a Band 6 Specialist Biomedical Scientist you must have your Specialist Portfolio in Haematology with (or without) Blood Transfusion or equivalent qualifications and experience which may include the BBTS Specialist Certificate in Transfusion Science Practice.
Person Specification
Experience
Essential
- A good understanding of the clinical significance of results and ability to interpret and act upon the results you are producing in a lone working setting
- Confident to make decisions in line with guidelines and written procedures to provide patient results including blood film morphology and special coagulation assays
Experience
Essential
- A good understanding of the clinical significance of results and ability to interpret and act upon the results you are producing in a lone working setting
- Confident to make decisions in line with guidelines and written procedures to provide patient results including blood film morphology and special coagulation assays
Experience
Essential
- A good understanding of the clinical significance of results and ability to interpret and act upon the results you are producing in a lone working setting
- Confident to make decisions in line with guidelines and written procedures to provide patient results including blood film morphology and special coagulation assays
Qualifications
Essential
- HCPC registration as a Biomedical Scientist with a Biomedical degree or equivalent and evidence of CPD, with post registration experience working in Haematology and proven ability to prioritise and manage own workload.
- To commence employment as a Band 6 Specialist Biomedical Scientist you must have your Specialist Portfolio in Haematology with (or without) Blood Transfusion or equivalent qualifications and experience which may include the BBTS Specialist Certificate in Transfusion Science Practice.
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).
