SHRISHTI J NARANG

Supported service users by implementing structured care plans, ensuring comprehensive and reliable documentation.

Demonstrated flexible working and clear communication, effectively managing varied demands in a dynamic support environment.

Performed immunoassay-based analysis on biopharmaceutical protein samples, strictly adhering to GMP-aligned facility standards and defined acceptance criteria.

Prepared and accurately labelled reagents and biological materials, ensuring full traceability and maintaining GCLP- and GMP-compliant batch records.

Operated diverse laboratory instruments following SOP-based procedures, ensuring safe handling of reagents and biological materials with appropriate PPE.

Maintained laboratory readiness through meticulous housekeeping, consumables restocking, and detailed recording of lot and batch information for full audit trail.

Executed serial dilutions, aseptic plating, and colony enumeration with high accuracy, recording results in SOP-aligned laboratory logs.

Performed PCR and agarose gel electrophoresis using strict aseptic technique, implementing contamination control protocols and safe handling of biological materials.

Prepared microbiological media, buffers, reagents, and solutions according to written procedures, ensuring full traceability through meticulous labelling and storage.

Operated and maintained diverse laboratory equipment, including centrifuges, PCR thermocyclers, and gel electrophoresis apparatus, supporting routine performance checks.

Conducted GC-El analysis of fatty acid samples, preparing reagents, operating equipment, interpreting chromatograms against acceptance criteria, and accurately recording results.

Maintained laboratory cleanliness via routine bench cleaning, glassware washing, equipment decontamination, and waste management in compliance with safe working practices.

Monitored and restocked laboratory consumables, meticulously recording batch and lot details to ensure full stock traceability in line with GMP expectations.

Completed accurate documentation for all testing activities, maintaining structured records in Microsoft Excel and SOP-aligned logs for audit readiness.

Collaborated effectively with laboratory teams to meet testing schedules, demonstrating flexibility and a quality-focused approach under varying priorities.

Maintained confidential clinical records with high accuracy, adhering to strict GDPR-compliant standards.

Supported document preparation in a fast-paced, regulated healthcare setting, contributing to efficient practice operations.

Provided patient and family support, demonstrating professional standards aligned to NHS requirements.