{"interviewQueryText":"What are some good interview questions in British English for the job description below?\n\n-------------------------------------------\n\nBand 8a Laboratory Manager- Blood Sciences with The Christie Pathology Partnership LLP in Manchester\n\n An exciting opportunity has arisen at The Christie Pathology Partnership (CPP) for a suitably qualified and experienced Laboratory Manager 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. Responsibility for Haematology, Biochemistry and Sample Reception. Organising and managing a team of Biomedical Scientists, junior staff and support staff performing Biomedical analyses and processes. Ensuring a high quality of analysis agreed quality standards of service delivery and key performance indicators. Providing an expert level of theoretical and practical knowledge to the laboratory service. Full details of the role can be found in the attached job description / job summary. The successful candidate will have: MSc or equivalent level of qualification (by examination) in Haematology/Biochemistry IBMS Higher Specialist Diploma in Haematology, Biochemistry or equivalent HCPC registered Biomedical Scientist Level 3 or above Management Qualification or equivalent experience. Advanced working knowledge of Haematology/Biochemistry techniques and practices post MSc level Excellent problem solving skills Highly developed leadership qualities To apply for this post you must be HCPC registered as a Biomedical Scientist and have a proven scientific and professional record. SYNLAB is a committed equal opportunities employer and we are open to flexible working. Applicants must currently have permission to work in the UK. About us Organise and manage teams of Biomedical Scientists, junior staff and Support staff performing biomedical analyses and processes, managing workload processing to comply with both Quality Standards and Key performance Indicators. This will be on more than one site or across specialisms. Maintain the standards of conduct required by the Health and Care Professions Council (HCPC) as a registered Biomedical Scientist Provide expert technical advice to clinicians as to the appropriateness of tests, timescales and scientific guidance as required. Have expert operational and technical knowledge to perform and manage specialist analytical procedures Ensure compliance with all policies as required by regulatory directives, accreditation bodies and local management, including; - UKAS - CPP policies and SOPs - MHRA - HTA - Any other body in area of responsibility Produce and manage Standard Operating Procedures (SOP). Manage the introduction of new technologies/processes and to maximise the benefits accrued To be responsible for External and Internal Quality Assurance in area of responsibility. Reporting on, and completing corrective actions required to address any areas of poor performance, including, where required, staff performance management. Ensure all documentation required for Quality Management System is recorded and maintained Plan and organise audits and audit calendar Chair/lead and/or participate in Technical, Training Quality , Audit and Management meetings, attendance at IT user groups as required 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. Plan and prioritise work allocations, training plans, for both yourself and junior staff, responding appropriately to the needs of routine and urgent activities. Provide management, training and professional leadership to staff in your area of responsibility, this includes monitoring their performance against laboratory standards and their training plans. Ensure that all equipment within area of work is maintained and operated as per SOPs. Be proficient in use of Integra and authorise orders against delegated authority policy. Management of consumables and conduct stocktakes in line with CPP policies To assist in Clinical trials in areas of responsibility as directed. Initiate changes in procedures or policies to induce service development, and continuous improvement. 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. Matters being communicated may include highly complex information and/or results. 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. Risk assessment and risk register monitoring according to CPP procedure/policies. 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. Safety: To observe safety regulations and attend mandatory fire, manual handling and other course as required and ensure all staff attendance is within required timeframes. 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 CPP policy for annual mandatory updates and have knowledge of COSHH and Lifting and Handling Policies "}