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Specialist Biomedical Scientist
4 months ago
Job summary
We currently have an exciting opportunity for a Band 6 Specialist BiomedicalScientist to join our Blood Sciences team at The Christie PathologyPartnership. The Christie is the largest single site cancer centre in Europeand the first UK centre to be accredited as a comprehensive cancer centre; withmore than 60,000 patients treated a year. This is full-time permanent role andyou will be expected to participate 24/7 rota.
Christie Research has more than 650 open trials and is the largestcentre in the UK for commercial cancer trials. It is a Cancer Research UK MajorCentre, part of the National Institute for Health Research (NIHR) BiomedicalResearch Centre, and hosts the NIHR Manchester Clinical ResearchFacility. The Trust is also one of the first wave of hospitals offeringCAR-T therapy on the NHS.
Main duties of the job
To be able to rotate through all areas of aLaboratory as required (dependent on qualifications, experience and training),to perform all designated duties in accordance with local working practices, tomaintain high Professional standards and conform to Health and Safetyregulations
To perform and interpret routine andspecialist biomedical investigations autonomously to provide patients resultswithin agreed quality standards of service delivery and turnaround times underthe supervision of senior staff
Work independently, implement and proposechanges to procedures for own work area. May be a lead specialist
To provide professional leadership andtraining to Basic Grade, Trainee BMS, Associate Practitioners (equivalentgrades) and Medical Laboratory Assistants
To provide specialist technical advice toclinicians as to the appropriateness of tests and timescales
About us
SYNLAB UK & Ireland work closely with clinicians, hospitals,occupational health providers and clinical researchers to provide a completepathology offering.
We operate in increasingly diverse environments which is reflected inour workforce, clients, customers, suppliers, communities and partners. Webelieve an inclusive workplace culture is the best way to source, attract andretain diverse and talented people, and create a sustainable, high-performing workforce.
We believe our staff is vital to the principle of making a positivedifference to healthcare, therefore, we promote a culture of continuouspersonal development where scientists and staff have the support and resourcesto acquire new skills and build their careers through learning and developmentopportunities, coaching and clear career pathways.
We reserve the right to close any adverts once we havereceived a sufficient number of applications. If you decide to apply for thispost but do not hear back from us within two weeks of your application, pleaseassume that you have not been short-listed on this occasion.
SYNLAB UK & Ireland is a committed equal opportunities employer anddoes not unlawfully discriminate on the basis of any status or conditionprotected by applicable UK employment law.
Job description
Job responsibilities
Participate in and assist withclinical trials, the development of new tests and research & validation ofequipment ensuring at all times compliance with all policies as required byregulatory directives, accreditation bodies and local management policies and practices.
To provide technical advice toclinical staff
To perform and interpret routine andspecialist Biomedical investigations and to participate daily in the scientificand technical activities of the laboratory section under the supervision ofsenior staff.
Together with Senior staff helpensure 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 Partnershippolicies and SOPs
-MHRA
-NHSCSP
-HTA
-HFEA
Any other body in area ofresponsibility
Utilise the laboratory LIMS, Q-Pulsequality monitoring system and other application software according toauthorised protocols including assisting in computer data entry in all areas ofthe laboratory, document review, non conformance review and quality assuranceprocesses.
Communicate efficiently, courteouslyand with clarity at all times, whether face to face, telephone or electronicmethods referring enquiries to senior staff where appropriate. Matters beingcommunicated may include complex information and/or results.
Attend and participate positively inlaboratory and other meetings as directed by Laboratory senior staff
As directed by senior laboratorystaff, plan and prioritise work allocations, training plans, audits of bothyourself and junior staff, responding appropriately to the needs of routine andurgent activities.
Encourage active participation incontinuous professional development and support the introduction of newtechnologies and / or systems by being a change advocate.
Report all incidents and adverseevents to senior staff and enter the information into Datix in a timely manner.
Demonstrate on going competencyagainst training plans and participate positively in CPD (continuousprofessional development) activities.
Safety:
To observe safety regulations andattend mandatory fire, manual handling and other course as required.
To assist in the investigations ofany incidents.
Participate in risk assessmentmonitoring
To ensure that the equipment withinarea of work is maintained and operated as per SOPs
To comply with The Christie policyfor annual mandatory updates and have knowledge of COSHH and Lifting andHandling Policies
Person Specification
Experience
Essential
At least 2 years relevant experience post HPC registration as a BMS with on-going specialist training
Qualifications
Essential
HCPC State Registration as a Biomedical Scientist in Blood Sciences discipline BSc (Hons) Biomedical degree or equivalent IBMS Specialist Portfolio or equivalent