Nashleen Karriem

Molecular Biologist and Research Assistant with over seven years of combined experience in molecular biology, microbiology, clinical research, quality control, and laboratory operations. Experienced in tuberculosis and infectious disease research, molecular diagnostics and biobanking within a Biosafety Level 2 and 3 (BSL) laboratory facility.

Research Assistant at CLIME Research Group, Faculty of Medicine and Health Sciences, Stellenbosch University (2023-11 – Present)

• Provide research support across multiple clinical and laboratory-based infectious disease projects.
• Coordinate specimen collection according to clinic schedules and research protocols.
• Perform sample logging, processing, extraction, aliquoting, storage and biobanking of clinical specimens and their derivatives.
• Trained to work safely in a BSL-3 facility while adhering to strict biosafety and quality standards.
• Maintain research databases and perform quality control checks, updating records, and implementing required modifications.
• Develop and update SOPs.
• Manage laboratory inventory, procurement and equipment maintenance.
• Train new laboratory staff and ensure compliance with GCP.
• Contributes to the implementation of improved laboratory systems and workflows that enhance efficiency and consistency.
• Collaborate with investigators, clinicians and multidisciplinary research teams.

Quality Control Scientist at Roche Diagnostics (2015-12 – 2019-05)

• Performed product quality control testing in accordance with approved SOPs and established turnaround times.
• Accurately recorded, analyzed and reported QC results using approved documentation and quality systems.
• Conducted ad hoc testing to support troubleshooting, investigations and test method validation activities.
• Performed routine maintenance, calibration checks and qualification of laboratory equipment used for QC testing.
• Maintained and updated QC protocols, SOPs and laboratory documentation.
• Drove and supported Non-Conformance Reports (NCR), Corrective and Preventive Actions (CAPA) and Change Control (CR) processes, including participation in root cause investigations.
• Performed routine monitoring of qualified systems to ensure compliance with quality and regulatory requirements.
• Executed qualification testing for QC equipment and supported method verification and validation activities.
• Ensured compliance with ISO quality management systems ISO 9001 and ISO 13485, GLP and laboratory safety requirements.
• Collaborated with cross-functional teams to achieve quality objectives while consistently meeting productivity and quality targets in a fast-paced laboratory environment.

Laboratory Demonstrator at University of the Western Cape (2013-03 – 2015-08)

• Prepared laboratory equipment and reagents for practical sessions.
• Conducted laboratory demonstrations and assisted students.
• Ensured laboratory safety and correct equipment usage.

Master of Science in Biotechnology – University of the Western Cape (2016)

BSc Honours in Biotechnology – University of the Western Cape (2012)

Bachelor of Science in Biotechnology – University of the Western Cape (2011)