Job Purpose: Under direct supervision, uses fundamental concepts, practices, and procedures, together with particular platforms, to perform routine clinical sample processing. These tasks may require the application of established techniques, procedures, and criteria. This includes the generation of revenue by conducting fee-for-service analyses of biological samples (e.g., blood, saliva, stool, urine, bacteria, etc) for external clients using various equipment (e.g., flow cytometers, centrifuges, incubators, analytical and statistical software, office equipment, etc.). Candidate must have flow cytometry experience. Main areas of responsibility: Develops and validates bioanalytical tests under the guidance of Scientists. Performs clinical sample analysis and clinical sample reporting. Ensures clear audit trails by performing quality control of all information and data generated. Assists with documents for projects (e.g., Lab Manuals, Validation Phase Plans, Method Development Plans, Sample Analysis Plans, Sample Analysis Reports etc.). Assists with multiple projects in a fast-paced laboratory environment. Management, monitoring and ordering of consumable stock thereby ensuring that sufficient reagents are available to perform assays. Stock takes (this includes stock management on a Laboratory information management system (LIMS)). Strong adherence to regulatory compliance and safety requirements involving good clinical laboratory practices (GCLP), standard operating procedures (SOP´s), Health & Safety policies, and other related documents. Assumes the responsibility of Study lead on projects as well as chief analyst on assay methods. Odoo timesheet and planning accurately and efficiently. Ad-hoc Writes and/or reviews/validates SOP´s, standard working procedures (SWP´s), documents, forms, and spreadsheets. Documents and updates the installation, operation, and performance qualifications (IQ/OQ/PQ) of equipment e.g., new equipment, preventative maintenance (PM), services etc. Ensures that equipment being used for assays are fit for purpose and are not used outside of service dates (equipment custodian). Performs set-ups, start-ups, and verification of various analysers (e.g., electrochemiluminescence analysers, microplate readers, flow cytometers etc.) and laboratory equipment (e.g., centrifuges, pipettes, timers, and thermometers etc.). Performs daily good housekeeping (GHK) duties. Completes and maintains relevant documentation related to clinical trials such as overview documents, sample logistics tracking forms, worksheets, and method sheets etc. Ensures correct, timeous, and documented receipt of all sample as well as reagent deliveries including proper storage thereof (this includes locating and drawing of samples and reagents when needed). Assist with the training of other staff members in company procedures and validated methods Skills and Competencies required: General understanding of bioanalytical & biomarkers services to provide support if needed. Excellent interpersonal skills Ability to drive and motivate internal stakeholders. Ability to prioritise tasks and manage time effectively. Detail orientated approach and ability to work well under pressure.