M*****h
About Candidate
Current Medical Laboratory Scientist with extensive experience in regulated healthcare operations, documentation accuracy, quality systems, and compliance workflows. Brings strong attention to detail, audit readiness, and protocol adherence, with skills directly transferable to a Clinical Research Associate role supporting study monitoring and regulatory compliance.
Regulated healthcare operations professional with over seven years of experience managing compliance-driven workflows, documentation control, and operational readiness in high-complexity clinical environments. Proven ability to coordinate quality systems, monitor regulatory performance, and design workflow processes that strengthen efficiency, accuracy, and audit preparedness. Brings a strong foundation in regulatory thinking, process improvement, and cross-functional coordination directly transferable to clinical research study activation and start-up operations
Nationality
Certifications
Associate of Science in Medical Laboratory Technology – Southern University at Shreveport
Medical Laboratory Scientist (MLS), AMT – 2024
Medical Laboratory Technician (MLT), ASCP – 2017
Looking for Job Title
Iqama
Location
Education
Work & Experience
• Direct daily operational readiness for a high-volume laboratory processing approximately 350 patient samples per day, ensuring workflow efficiency, regulatory compliance, and result accuracy. • Lead startup and validation processes for five analyzers daily, confirming QC acceptance, calibration status, reagent stability, and documentation completeness prior to testing. • Monitor QC performance and analytical trends daily, identifying shifts, assay instability, and calibration failures to mitigate regulatory risk and reporting errors. • Maintain complete, audit-ready documentation including QC logs, calibration records, maintenance reports, and inventory controls. • Design and implement department-specific workflow schedules improving turnaround time and accountability. • Develop and manage an inventory ordering system stabilizing reagent availability and reducing testing interruptions. • Create an autoimmune testing tracking schedule to improve sample prioritization and traceability. • Train and mentor five staff members on analyzer startup, QC interpretation, documentation standards, and SOP compliance. • Serve as primary operational contact for troubleshooting QC failures and workflow disruptions. • Act as liaison between laboratory staff, leadership, and support teams.
environment. • Reviewed assay documentation, QC results, and validation materials ensuring compliance with validated methods. • Maintained complete run documentation supporting data traceability and audit readiness. • Assisted with troubleshooting assay performance deviations and ensured corrective documentation accuracy. • Collaborated with multidisciplinary teams to ensure SOP adherence, data integrity, and turnaround performance. • Supported inspection readiness by maintaining organized regulatory documentation.
