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Liza Bhusal

Liza Bhusal is a microbiology graduate with a strong foundation in laboratory science, quality control, and applied microbiological analysis. She is currently doing her M.Sc. in Microbiology at GoldenGate International College and completed her Bachelor of Science degree in Microbiology from GoldenGate International College, Tribhuvan University, where her coursework covered medical microbiology, molecular biology, immunology, genetics, biostatistics, and microbial physiology. Her academic project focused on the microbiological analysis of the external auditory canal in healthy individuals with varying hygiene and earphone use habits. Liza previously worked as a Quality Control Technician at the Fred Hollows Intraocular Lens Laboratory, Tilganga Eye Center. In this role, she performed routine quality inspections of intraocular lenses, ensuring compliance with ISO 13485 standards and internal quality systems. Her responsibilities included defect identification, documentation of test results, calibration support, and collaboration with production and quality assurance teams to address nonconformities and support continuous improvement. Her technical skills include aseptic technique, microbial culturing, staining, microscopy, biochemical testing, GMP-aligned workflows, and audit-ready documentation. She also holds certification in Good Clinical Laboratory Practice and has basic training in digital marketing and data handling tools.

Importance of Traceability and Documentation in QC Labs

May 5, 2026May 2, 2026 by Liza Bhusal
Importance of Traceability and Documentation in QC Labs

Traceability and documentation are of utmost importance to ensure comparable results, support investigations, and meet regulatory requirements. Reliable quality control (QC) data is the backbone for safe medicines, valid diagnostics, … Read more

Handling Nonconformities in Medical Device Production

May 5, 2026May 1, 2026 by Liza Bhusal
Handling Nonconformities in Medical Device Production

Nonconformities in medical device production are any deviations in process or product from specified requirements. Managing nonconforming products is essential for medical device quality, patient safety, and regulatory compliance. Standards … Read more

Aseptic Techniques in Medical Device Quality Testing

March 15, 2026 by Liza Bhusal
Aseptic Techniques in Medical Device Quality Testing

Aseptic techniques in medical device manufacturing are crucial processes to protect products from contamination by microorganisms throughout production and quality control tests. Overview of Aseptic Techniques The sterilization process kills … Read more

Cleanroom Practices in Medical Device Manufacturing

March 12, 2026 by Liza Bhusal
Cleanroom Practices in Medical Device Manufacturing

Medical device manufacturing is a sensitive process, and for devices such as implants and pacemakers, even a small amount of contamination by dust, microbes, or skin cells poses a significant … Read more

Good Manufacturing Practices (GMP) in Medical Device Labs

March 5, 2026 by Liza Bhusal
Good Manufacturing Practices (GMP) in Medical Device Labs

Good Manufacturing Practices (GMP) are essential, globally recognized guidelines that ensure medical devices are consistently produced, safe for patients, fit for use, and comply with relevant regulations. It ensures products … Read more

Introduction to ISO 13485 for Medical Devices

February 25, 2026 by Liza Bhusal
ISO 13485 for Medical Devices

The medical device industry is a highly regulated and closely monitored sector where various guidelines and regulatory standards must be adhered to. ISO 13485 is a medical device-specific Quality Management … Read more

Quality Control vs. Quality Assurance in Medical Devices 

February 22, 2026 by Liza Bhusal
Quality Control vs. Quality Assurance in Medical Devices

The major component to consider for any product is its quality. Quality, in its simplest term, is how good or bad a product is. However, “quality” for medical devices is … Read more

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