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Specialist Biomedical Scientist- Haematology and Blood Transfusion with iPP Analytics Limited in Basildon, Essex
We are seeking an enthusiastic and motivated Specialist Biomedical Scientist in Haematology and Transfusion to join our Blood Sciences team based in Basildon with flexibility to work at the Southend site. Pathology First operates over three sites using a hub and spoke model. Our hub site offers a high throughput service for our non-urgent community work, and specialist testing comprising factor assays, haemoglobinopathy screening and flow cytometry. Our two hospital laboratories at Southend and Basildon provide urgent testing for acute admissions and inpatients with a full hospital transfusion service, this includes serving the cardiothoracic centre at Basildon, and a substantial oncology and haemato-oncology workload. The Southend site boasts a biomedical scientist-led anticoagulant clinic. This role will involve rotating across the haematology and transfusion sections and across sites. Our laboratories receive approximately 1.2M FBC and coagulation samples and 100K transfusion samples per year. The department is equipped with Werfen ACL-TOPs, Beckman Coulter DXHs, Ortho Visions and Bio-Rad D100s. The main IT platform for all sites is Clinisys WinPath Enterprise. The role will require a high degree of biomedical scientific skills and process knowledge.You will work with managers to ensure the successful delivery of new solutions, and implementation of service and process improvements to the required quality, within budget and deadlines. You will need to be flexible to fit in with our multi-site, around the clock shift pattern (unsocial shifts attract additional payments). The environment is fast-paced offering a one-hour turnaround time to acute users, two hours for inpatients and four hours for community requests. You will require specialised knowledge and experience of laboratory techniques, analyser platforms and associated equipment. You will have a role in the training of less experienced employees, and you will be involved in quality management including auditing and document review. Qualifications and experience: HCPC registered as a Biomedical Scientist IBMS Specialist Diploma in Haematology with Hospital Transfusion Practice, or in Haematology only with separate BBTS certificate, or equivalent specialist qualifications Able to work across three sites as required, including hospitals which operate 24-hours Able to work with a high degree of accuracy, numeracy, interpretive skills, and good problem-solving skills Able to demonstrate a good knowledge and experience of industry standard laboratory information management systems Specialist knowledge of Haematology and Transfusion techniques and practices About us Integrate with the Operational Management Team to share ideas and improve operations, recommending, supporting, and implementing continuous improvement activities and process and procedure improvements to optimise results and improve quality of delivery. Responsible for working with managers to identify, develop and implement business improvement opportunities across Blood Sciences, ensuring delivery against their associated outcomes. Perform Biomedical analyses and processes, managing workload processing to comply with both Quality Standards and Key Performance Indicators. Undertake business process analysis and statistical analysis for improvement projects to support wider change. Manage the introduction of new technologies/processes and to maximise the benefits accrued. Support the creation of a culture that embraces managed change and continuous improvement through acting as a role model for transformation and sharing those skills to empower local teams. Work collaboratively with staff and key stakeholders to ensure engagement participation in the planning, progress and completion of changes. Proactive management and containment of risks, assumptions, issues, and dependencies, ensuring successful delivery of change and minimum disruption to business continuity. Ensure project scope, goals, benefits, and deliverables are defined. Ensure appropriate monitoring of change initiatives through KPIs aligned to wider business objectives. Plan and prioritise work allocations, training plans, for both yourself and junior staff, responding appropriately to the needs of routine and urgent activities. Provide training, and professional leadership to staff in your area of responsibility, this includes monitoring their performance against laboratory standards and their training plans. Coach and facilitate teams and individuals to identify and implement improvement opportunities. Ensure compliance with all policies as required by regulatory directives, accreditation bodies and local management, including; - Healthcare Professions Council Accreditation (HCPC) - Pathology First policies and SOPs - MHRA and any other body in area of responsibility Produce and manage Standard Operating Procedures (SOP) 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. Maintaining software systems and updating as required. Track milestones and deliverables effectively and report and communicate progress to stakeholders. Report and investigate all incidents and adverse events entering the information in the CAPA module of Q-pulse in a timely manner, conducting Root Cause analysis and remedial action as required. Chair/lead and/or participate in Technical, Training Quality, Audit and Management meetings as required. Attendance at LIMS user groups as required. Be proficient in use of ERP system (Axional) Maintain the standards of conduct required by the Healthcare Professions Council (HCPC) as a registered Biomedical Scientist. Demonstrate on-going competency against training plans and by peer assessment and participate positively in CPD (continuous professional development) activities through academic or practical experience. Other: Be an ambassador for Diversity and Inclusion. Communicate and role model the values and behaviours of SYNLAB. Communicate efficiently, courteously and with clarity at all times, whether face to face, telephone or electronic methods referring enquiries to senior staff where appropriate. To undertake any other reasonable duty, when requested to do so by an appropriate manager. Safety: To observe safety regulations and attend mandatory fire, manual handling and other courses as required. Report all incidents and adverse events to managers and 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 SYNLAB policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies