Onyinyechukwu Aneke

I am passionate about working as a biomedical scientist and have gone through the job description and person’s specifications I meet the essential and most of the desirable criteria hence, I am a perfect match for the role. Also, with a strong foundation in biomedical science and substantial experience in blood sciences, I am well-positioned to excel as a Biomedical Scientist at your Trust. I hold an Institute of Biomedical Science (IBMS) accredited degree in medical laboratory science, and happy to start the specialist portfolio immediately.

I am registered with the Health and Care Professions Council (HCPC). My expertise spans a range of disciplines, including haematology, blood transfusion, clinical chemistry, immunology, tumour markers, drug toxicology, and special proteins, with significant experience in the use of various blood science analysers such as Roche, Mindray, Beckman, Abbot, and Sysmex. My extensive knowledge in these instrument maintenance, verification and validation further underscores my suitability for this role.

I have confidence in my ability to handle complex analytical tasks, operate and maintain sophisticated analysers, and contribute meaningfully to the diagnostic pathway. I have understanding of both the technical and professional standards expected. I am ready to bring with me a strong work ethic, a growth mindset, and a commitment to delivering safe, accurate, and compassionate patient care.

Throughout my career, I have demonstrated a capacity to perform complex biomedical procedures, including the use of sophisticated analysers and following complex SOP, without supervision. I have actively contributed to the quality management system within my department, ensuring compliance with ISO 15189 and MHRA standards, and have been involved in audits, evaluations, and clinical and information governance. My experience extends to implementing and adhering to quality management systems, where I have effectively utilised internal and external quality control measures to maintain and elevate laboratory standards.

I have been actively engaged in the development and review of Standard Operating Procedures (SOPs) and have overseen their implementation using systems like WebV, APEX, which is essential for maintaining a robust quality framework in the laboratory environment. I am skilled in managing the day-to-day operations of a pathology laboratory, ensuring the delivery of a high-quality, efficient, and effective service. I have supported senior laboratory biomedical scientist staff in implementing change and enhancing service delivery, contributing to the department’s overall performance through continuous quality improvement initiatives.

My responsibilities have included handling the technical aspects of service delivery, such as maintaining equipment, monitoring performance, and managing external quality assessment (EQA) schemes. I am experienced in troubleshooting and resolving non-conformities identified through internal and

Biomedical Assistant at Northern Lincolnshire and Goole NHS Trust Foundation (2025-08 – Present)

• Performance of accurate analysis of samples using specialist instrumentation or ‘manual techniques’ after reception of appropriate training on all pieces of equipment expected to be used in discharge of duties. This includes an understanding of the basic construction of the equipment, knowledge of moving parts, and an understanding of computer software used on the analyser.
• To recognise and report any process or assay failures to the appropriate person. Identify faults and perform routine maintenance / set-up on automated equipment and maintain accurate records which includes automated analysers and the use of calibrated equipment to make accurate measurements, such as pipettes.
• Equipment checks, including periodic maintenance and checking of equipment, ensuring that they meet laboratory standards involving high degree of manual dexterity, utilizing fine tools requiring accuracy and concentration.
• Make accurate dilutions of samples and reagents using precision pipettes.
• Undertake appropriate training and gain the necessary knowledge to use Laboratory Information (APEX, WEB V3) and Management Systems including the entry of test results and the generation of test worksheets and outstanding work lists.
• Storage of patient samples, stained slides, electrophoresis plates and all documentation securely and correctly according to the Laboratory Retention policy.
• Stock management, including the recording of reagent stocks as they are delivered into the laboratory.
• Perform weekly stock-take to identify reagents etc. required. To record this data on a standard spreadsheet and report any stock shortfalls.
• Chemical reagent preparation and replacement as appropriate to the department.
• Removal of clinical waste in bags from Pathology, on a daily basis, to a secure clinical waste skip.
• The use of effective communication skills with Pathology staff and users of the service.
• Dealing with telephone enquiries and provision of results.
• Receipt of specimens, sample identification and numbering including initial investigation of missing/lost or mislabeled samples, requesting repeat samples where necessary.
• Work file enquiry generation, investigation of pending work including location and testing of any missing samples. Advising the service users of any discrepancies where appropriate.
• Record keeping, including recording the temperatures of refrigerators, freezers, water baths, incubators etc. where appropriate.
• Use of scanning software to archive paper records.
• Secondary preparation and processing of samples for referral to other laboratories.
• The operation of complex, specialised and valuable equipment – including sample processing, quality issues, instrument set-up and maintenance, reagent replacement, quality control.
• To recognize any system failures and report these to the registered BMS staff. Some of the analyser maintenance procedures also involve the use of fine tools and require precise accuracy / concentration.

Phlebotomist/Medical Laboratory Assistant at Northern Lincolnshire and Goole NHS Trust Foundation (2024-12 – 2025-08)

• Collection of blood samples from patients through venepuncture (phlebotomy) in an Outpatient (clinic) facility and in Inpatients including collection from the acute wards. All samples are collected as per Trust guidelines.
• Collection of blood from the arm in order to achieve good quality samples based on choosing the correct vein from which to draw blood.
• Awareness of the specific requirements for some tests e.g. fasting, resting, and the performance of multiple timed collections e.g. Glucose and Lactose tolerance tests.
• Having great attention to detail required in the correct identification of patient, using full name and date of birth, and wrist bands for inpatients, and also ensuring that samples are drawn in the correct order for optimal analysis.
• Ensuring that samples are legibly labeled by hand in accordance with the Trust labelling policy.
• Ensuring all samples must be delivered to the laboratory in a timely manner.
• Delivering excellent communication skills as required due to the high level of patient contact, ensuring that patients' concerns about the physical requirements of venepuncture are cleared while reassurance or further information are given as due.
• Ensuring that professional and courteous manner is maintained at all times.
• Making sure that stock management, including the replenishment of phlebotomy stock and advising line managers when stock levels are low is constantly updated.
• Receipt of specimens, sample identification and numbering, as well as initial preparation of samples for processing, including use of centrifuges where appropriate.
• Entry of patient and specimen data onto laboratory data systems.
• regular maintenance of professional standards, by participation in training offered, including CPD, and keeping up to date with current practice.
• Ensuring that personal competency records are up to date, which includes an understanding of the basic theory and practical knowledge of phlebotomy.
• Maintenance of confidentiality of information gained in the execution of duties.
• Compliance with Health and Safety legislation, and Trust and Departmental H&S Policies and attending mandatory training sessions.
• Familiarization and adherence of Trust policies and procedures.

Laboratory Technician at Eurofins Food Testing UK Ltd (2024-07 – Present)

• To complete the relevant testing stage to the required standards and internal methods/procedures. Further, assist in the efficient day-to-day operation of the laboratory.
• Adhering to SOPs for the relevant section of the laboratory, ensuring that all pertinent information concerning samples is recorded, that samples are handled correctly, and that all necessary records and quality data are maintained.
• Responsible for ensuring that UK health and safety legislation is maintained and helping to ensure that the working environment is kept tidy at all times with due attention to laboratory fittings and equipment.
• ensure that PPE is worn at all times.
• work with the team to drive the laboratory forward through continuous improvement.
• knowledge of the Laboratory Quality Manual to ensure compliance at all times with the policies, procedures, and associated documents that are referred to in the manual.
• assist through operating best practices to meet the requirements of the UKAS accreditation standard.
• Provide a high level of internal and external customer care.
• Responsible for promoting a professional image of the company and for complying with the company's Equal Opportunities and Harassment policies at all times, including work-related events that take place outside normal working hours.
• read and comply with company rules, procedures, agreements, and any notices displayed by the company.
• Any other reasonable tasks as delegated by the team leader/Line manager.
• To carry out registration and processing of samples in line with the quality standards and methods using eLIMS.
• To carry out media preparation, plate reading/confirmation tests in line with quality standards, and written procedures.
• To carry out media QC, IQC, and environmental monitoring in line with the standards.

Biomedical Scientist at Simaug Hospital and Maternity, Enugu, Nigeria (2023-07 – 2024-02)

• Assist the laboratory manager to ensure a safe working environment per relevant legislation and all safety protocols. This includes the ongoing maintenance of quality control standards, adherence to infection control measures, correct disposal of bio-hazardous waste, and the preparation process for internal and external audits.
• Performs diagnostic testing procedures, reviews and verifies results, and interacts with pathologists on technical matters to provide all relevant data that may pertain to the prevention, diagnosis, or treatment of diseases.
• Assist the laboratory manager to ensure that incidents and instrument failures are reported by laboratory staff, thereby ensuring compliance with relevant organizational policy and laboratory standard operating procedures
• Manage client liaison to maintain a positive image of the organisation, promote the services of Cerbalancet laboratories and monitor resolution of customer complaints
• Attends training and seminars and participates in continuing professional development (CPD) activities to continuously update knowledge and skills as well as comply with professional registration requirements. This includes ensuring the availability of up-to-date records that can be presented immediately on request thereof.
• Adheres to professional conduct requirements in line with the organisational policy and relevant professional body ethical standards.
• Liaise with laboratory manager and suppliers regarding QC errors, changes, and problems, to ultimately ensure the quality of results.
• Generation of the report on reference range verification when new tests or methods are implemented to ensure correct reporting ranges
• Management of Intra and Interlaboratory programmes and generations of reports, to statistically analyse the results for acceptability.
• Assist in the setup of the Biorad Unity Real-Time (URT) system to ensure the QC data is being uploaded into the programme to be monitored and evaluated against peers.
• Ensures the implementation of service levels and quality standards following standard operating procedures and service level agreements
• Records and verifies test results to ensure the integrity of the test result database on the laboratory information system
• Review and troubleshoot where needed IQC and EQA results from RIQAS, Thistle or any other external proficiency programmes.

Biomedical Scientist at University of Nigeria Teaching Hospital, Enugu, Nigeria (2020-10 – 2021-09)

• Apply principles and applications of Quality Management Systems (QMS) and participate in internal and external Quality Assurance schemes, reviewing external quality results of various clinical chemistry and immunology test samples and troubleshooting as needed.
• Review and validate results in accordance with standard operating procedures while using the Labware Laboratory Information Management System (LIMS)
• Assist during the ISO audit process.
• Liaised with other Randox Laboratories on best practices on analyser optimisation, Lot to lot-to-lot validation, etc.
• Utilised the Randox Stock Dashboard to document stock in and stock out of reagents, calibrators, controls and other laboratory essentials to ensure availability at all times.
• Process large daily blood sciences samples covering a range of clinical chemistry and immunology tests.
• As an advanced user, operate, maintain and quality control a wide range of analysers.
• Train and supervise junior colleagues.
• Upload and analyse IQC data on the BioRad QC platform.
• Coordinate quality processes such as Corrective and Preventive Actions (CAPA) in cases of non-conformance or significant incidents within the laboratory.
• Apply expertise in processing chemistry and immunology test profiles including tumour markers, special proteins, urine chemistry and drug toxicology.
• Demonstrate proficiency in performing therapeutic procedures such as plasma exchange, red cell exchange, and stem cell collection in the field of clinical apheresis.
• Demonstrate excellent organizational, interpersonal, and management skills, adhering to Trust values and maintaining professional relationships with staff at all levels.
• Uphold strict health and safety standards, follow COSHH and MSDS guidelines for chemical handling, and demonstrate competence in risk assessment and control.
• Provide quality, timely, and accurate diagnostic results for effective healthcare delivery while ensuring patient confidentiality and adhering to data protection acts and regulations.
• Display physical capability to handle 24-hour shift duties, including holidays, and welcome constructive feedback to enhance performance.
• Assess the suitability of specimens received for processing.
• Follow established health and safety procedures, including the proper use of Personal Protective Equipment (PPE), and ensure compliance with fire and other hazard/symbol regulations.

Biomedical Scientist at Family Support Project (FSP) Clinic alias Women's Affairs (2022-04 – 2023-03)

• Performance of qualitative and quantitative estimation of analytes on whole blood, serum, or plasma following Standard Operating Procedure (SOPs) in line with manufacturer’s instruction.
• Carried out all diagnostics tests solely past work hours during weeks of staff shortage due to sick days, maternity leaves of absence, and community health outreach.
• Supported other sister facilities in need of my services during clinic days when there is staff shortage with official permission from my laboratory manager.
• Ensuring that all results were validated and verified by authorised staffs before reporting on LIMS (Laboratory Information Management System) at the end of a day’s work in order to provide stable availability to pathologists.
• Ensured that collection, registration, and reporting using two identifiers, ID, age and sex to avoid minimal repeat of venepuncture/recollection of samples from patients, and preventing the rise of inappropriate samples discard due to wrong sample or anticoagulant container and also resolving erroneous requests with patients/wards/staffs when happen to issues arise in a calm manner.
• Performance of quality controls, calibrations, internal and external quality assurance (EQA) on all analysers in clinical chemistry and haematology departments to evaluate quality compliance with BIORAD safety and risk-management guidelines.
• Effectively assess and document all pre-analytical, analytical, and post-analytical errors and also take corrective measures using laboratory protocol when quality assurance evaluation shows deviation and then report findings to the laboratory manager.
• Ensured adequate communication of all critical results or problems to the physicians through telephone while documenting all corrective advice and action procedures undertaken in the department during my shift according to laboratory standard operating procedures.
• Assist in donor drives by establishing and updating voluntary donors register and ensure donors' safety with follow-up calls in the blood bank to ensure all blood bags are adequately screened and on standby for cross-matching and transfusion during childbirth or surgeries.
• Carried out training and supervision of new staffs, medical laboratory technicians on departmental procedures and guidelines, performing yearly stock audit, monthly record of stock and placing purchase order for procurement and IT skills training on LIMS thereby ensuring the laboratory polices, code of conduct and professional guidelines are of the facility were duly observed.
• Manage departmental stock, procure reagents and consumables, and ensure reagent quality by performing reagent validation and system check and appropriate reagents are received.
• Ensured Health, Safety and Equipment (HSE) was maintained in the department based on my training by providing PPE, waste bags, sharp containers, waste segregation management, and proper disposal methods according to laboratory policy. I adequately responded immediately to fire emergencies and unsafe act and conditions such as needle stick injuries, spillage, and near-miss were reported earlier.

Bachelor of Medical Laboratory Science (BMLS) in Medical Laboratory Science – Madonna University, Elele, Nigeria (2019)