Quality Manager

This job is brought to you by Jobs/Redefined, the UK's leading over-50s age inclusive jobs board.Company DescriptionSource BioScience is an international genetic analysis, diagnostics and stability storage business serving the global research and healthcare markets. We pride ourselves on maintaining a friendly working culture that gives driven individuals the environment to succeed in an evolving and developing organisation.Job DescriptionThis is a full time role based on site in Chichester.Closing date 31 August 2025Successful candidates will be required to provide references and are subject to a DBS Check prior to starting.Due to the volume of expected applications we reserve the right to close this advert prior to the closing date, we apologise that we are unable to respond individually to each application. If we have not contacted you within 7 working days your application has been unsuccessful and your details have not been retained. Please feel free to apply for any other position you may see in the future.The role has responsibility for the day-to-day management of the quality management system within Source BioScience, as well as supporting wider operation of quality across all sites within the business and will be critical for driving continual improvement across the company via feedback from the management system.The Source BioScience quality management system is in place across the Cellular Pathology/Healthcare (Source LDPath) and Genomics (Source Genomics) business units, and incorporates accreditation to ISO 15189 and ISO 9001, Good Clinical Practice (GCP), and registration with the CQC and HTA. The focus of the role will be cellular pathology and ISO 15189 accreditation but will support quality across all areas of the business.This role will support the Head of Diagnostics Development & Quality in the ongoing delivery of quality management using Q-Pulse software, maintaining ISO 15189 and ISO 9001 accreditation, other relevant standards and ensuring regulatory compliance with CQC, MHRA, HTA and any other relevant regulators.You will have a high level of responsibility to ensure the successful delivery of pathology and genomics services through effective management that meets the needs of users, in line with our company vision and quality objectives.Source BioScience has locations in Nottingham, Cambridge and Chichester, providing diagnostic healthcare services (cellular pathology and molecular diagnostics) and genomics services to industry and academia. The position is based at the Orchard Place site in Nottingham, but following discussion could be based in Chichester should this be preferential for the candidate. The role will require infrequent visits to other sites in the business as and when required (e.g., performing audits).QualificationsPerson Specification:Minimum requirements:Experience of operating and being responsible for management systems within pathology laboratories to ISO 15189 standards.Minimum 2 years' experience in either ISO 15189, ISO 9001 or ISO 17025 accredited environments.Auditing experienceExperience and understanding of root cause analysisHCPC registered Biomedical Scientist statusDesirable:Qualification in quality managementExperience of cellular pathology, molecular techniques, sequencing and genomics.Experience with GCP/clinical trialsFamiliarity with Q-PulseExperience in risk management, ISO 27001 or DCB 0129/0160Day to day management of the quality system at the Courtyard Laboratory and supporting implementation, consisting of:Performing audits of the management system, managing the audit schedule and making sure this is complete on time for The Courtyard Laboratory.Management of the Q-Pulse eQMS system:Workflow module (incident reporting/CAPA).Audit ModuleDocument moduleCustomer & Supplier modulesAsset modulesAdministrationProcess improvement and incident & complaint management.Incident investigation and root cause analysis, including supporting other departments in the business to complete investigations appropriately, ensuring corrective and preventive actions are effective.Writing, and review of quality policies, SOPs and documents.Quality review and approval of documents across the business and ensuring appropriate document control is implemented.Ensuring the validation and verification policy is adhered to, ensuring there is a process in place for performing equipment, procedures, methods and software validations/verifications and maintaining in a validated state.Support the Clinical Risk Management process through integration into the management system and management of risk assessments and failure modes effects analysis.Contributing to the Annual Management Review (AMR) and preparing quality reports.Produce monthly quality reports, reporting on KPIs and quality objectives for The Courtyard Laboratory.Supporting the business in achieving quality objectives - ensuring these are set, monitored and actioned.Co-ordinating the internal awareness of the needs and requirements of the users through the AMR, assessment and audit feedback, complaints, incidents and KPI/quality objectives.Provide training for staff undertaking quality related activities, as required. (e.g., training in performing audits and root cause investigation).Liaise with, lead and support accreditation and certification assessment visits and responses at The Courtyard Laboratory.Support any third-party audits by regulators or clients.Supporting quality leads within departments and at other sites within the business, with occasional travel if necessary (such as performing audits).Provide training for quality leads and any other staff undertaking quality related activities, as required.Deliver the expectation of the service users whilst also balancing the interests of the company.To lead by example, demonstrating professionalism to colleagues commensurate with post.To comply with safe working practises in accordance with Company safety policiesTo participate in the Annual Joint Staff Review process, in accordance with Company Policy.To perform any other duties as may be reasonably required commensurate with grade and experience.Attend any training endeavours as appropriate to the role or as reasonably requested by Line Manager.Additional InformationIncome ProtectionLife Assurance x4 salaryEmployee Assistance ProgrammeMedicash health cash planShopping & leisure discount portalVirtual GP ServicemProve Yourself health and wellbeing resourcesSkinVision AppAble Futures Mental Health support33 days holiday (inclusive of bank holidays) increasing with LOSAn extra day off on your birthdayOption to buy and sell holidaysCycle to work scheme #J-18808-Ljbffr