Alexus Martin

• Perform comprehensive specimen processing and clinical testing in accordance with SOPs, CLIA, CAP, and cGMP standards.
• Accession, verify, label, aliquot, and store specimens (blood, urine, swabs, tissue) to ensure integrity and traceability.
• Conduct clinical laboratory testing in urinalysis and chemistry, including toxicology screening and specialized procedures such as post-vasectomy sperm analysis.
• Operate and maintain high-complexity analyzers (Vitros 5600, AUTION MAX AX-4030, iQ Workcell 200), centrifuges, incubators, and microscopes; perform manual microscopy as needed.
• Execute quality control, calibration, troubleshooting, and preventive maintenance to maintain instrument reliability and compliance with regulatory standards.
• Package and ship biological specimens domestically following IATA and DOT regulations.
• Maintain chain-of-custody and achieve >99% accuracy in specimen documentation using the Laboratory Information System (LIS) and EMR.
• Prioritize STAT and critical samples to ensure timely, accurate results for urgent patient care decisions.
• Correlate laboratory results with clinical findings to verify abnormal results and resolve diagnostic discrepancies.
• Communicate effectively with healthcare providers, reference laboratories, and logistics vendors to resolve issues and support patient care continuity.
• Support internal audits, CAP inspections, and quality improvement initiatives.
• Trained and mentored new staff on specimen processing, instrumentation, and quality control protocols, ensuring regulatory compliance and operational consistency.
• Improved workflow efficiency by redesigning the specimen intake process, reducing processing errors by 20%.

• Performed daily morning quality control, powered on, calibrated, and verified readiness of laboratory equipment prior to patient testing.
• Prepared reagents and conducted clinical laboratory testing, including hematology CBCs, chemistry panels on automated analyzers, and urinalysis (dipstick and microscopic).
• Verified patient identity, insurance information, test orders, and provider details prior to specimen processing to ensure accuracy and regulatory compliance.
• Accurately documented all testing procedures and results in accordance with laboratory standards, CLIA, and CAP requirements.
• Recognized and reported critical laboratory values promptly to providers to support timely oncology treatment decisions.
• Applied critical thinking to troubleshoot instrument malfunctions, resolve technical issues, and correct clerical discrepancies prior to result release.
• Maintained consistent professionalism, accountability, and reliability while working in a high-volume oncology laboratory environment.

• Performed patient check-in and specimen intake in a high-volume clinic and military medical treatment facility, ensuring accurate patient identification and workflow coordination.
• Utilized Genesis (LIS) to manage patient records, specimen tracking, and laboratory workflow in compliance with HIPAA and laboratory protocols.
• Performed venipuncture on patients ages 11 and older, ensuring proper technique, patient comfort, and specimen integrity.
• Collected, labeled, and processed laboratory specimens in accordance with SOPs, CLIA, and CAP standards.
• Conducted point-of-care testing, including urinalysis and mail-out specimen processing, ensuring accurate and timely results.
• Maintained complete and accurate documentation for all specimen collections, testing, and patient interactions.
• Managed laboratory communications, including incoming calls and faxes, to support coordination between providers and laboratory staff.
• Maintained laboratory inventory and restocked supplies to ensure uninterrupted clinic operations.

• Assisted Hospital Corpsman Officers with administrative procedures, emergency treatment, infection control, laboratory testing, patient assessment, and medical documentation.
• Managed and inventoried medical equipment and supplies, ensuring operational readiness and compliance with safety protocols.
• Performed venipuncture on service members and accurately collected, processed, and documented blood specimens.
• Conducted routine and STAT point-of-care testing, including chemistry panels, microscopic urinalysis, KOH and wet prep microscopy, Beta HCG, rapid strep, and COVID-19 tests.
• Reported critical patient results promptly to providers within required timeframes.
• Maintained high standards of cleanliness through scheduled deep-cleaning procedures and adherence to infection control protocols.
• Ensured compliance with The Joint Commission (TJC), College of American Pathologists (CAP), and CLIA standards while following laboratory safety procedures.
• Provided guidance, technical support, and training to shipboard and clinical team members, fostering a safe and efficient work environment.

• Performed specimen collection, handling, processing, and test analyses across all major areas of the clinical laboratory, including hematology, chemistry, immunology, serology, microbiology, and urinalysis.
• Maintained accurate documentation and reporting of test results in compliance with laboratory quality control and assurance policies.
• Documented and conducted QC activities for urinalysis, hematology, and chemistry benches, ensuring accurate test performance and results.
• Identified potential indicators affecting test performance; applied corrective actions or escalated issues to the Lab Supervisor.
• Conducted daily equipment checks and calibrations before beginning each shift, supporting compliance and operational readiness.
• Coordinated orders and communications between the lab and outside laboratory facilities, ensuring accurate and timely specimen transfers.
• Answered and directed incoming calls and faxes for the core laboratory, providing timely information to patients, providers, and staff.
• Applied laboratory safety procedures and quality assurance practices to maintain a secure, compliant work environment.
• Delivered professional, warm, and friendly customer service while fostering teamwork and a positive workplace culture.

Detail-oriented Blood Donor Technician and Supervisor with 3+ years of experience in blood collection, donor care, and blood product manufacturing. Proven track record of processing 20+ donors per day, maintaining 99% compliance rates, and achieving error-free audits. Skilled in training staff, regulatory compliance (FDA, cGMP, CLIA, CAP), and ensuring high-quality donor and patient outcomes.

Blood Product Manufacturing Supervisor (Jan 2020 – Dec 2021)

• Supervised daily operations in manufacturing of blood products, including plasma, RBCs, and leukocyte-reduced units.
• Trained and mentored staff, ensuring adherence to SOPs, cGMP, FDA, CLIA, and CAP regulations.
• Oversaw QC, calibrations, and documentation with zero audit findings and 99% compliance rates.
• Coordinated workflow to support 20+ donors per day, ensuring safe, timely processing.
• Revised Laboratory Procedure Manuals and authored SOPs to align with regulatory requirements.

Blood Donor Technician (Jan 2018 – Dec 2019)

• Registered and screened an average of 20 donors daily, performing health history reviews, vital signs, and hemoglobin checks.
• Collected whole blood and monitored donor safety, providing post-donation care and education.
• Processed blood products with strict adherence to quality and regulatory standards.
• Performed routine QC and equipment checks with error-free audit results.
• Delivered professional, compassionate customer service while handling adverse donor reactions.