akilla User

Advised patients on OTC medications and maintained compliance with healthcare and GMP-related handling, achieving 100% in a compliance audit while streamlining stock rotation to reduce wastage by 10%.

Maintained health, safety and hygiene standards in a high-volume environment and supported team operations to meet production and service goals with minimal supervision.

Performed routine and non-routine QC testing on 15+ samples daily across raw materials, in-process, finished products and stability samples, and supported method validation and GC projects that improved accuracy by ~25%. Maintained instruments, authored SOPs, and contributed to OOS/OOT/CAPA investigations, increasing operational efficiency by 15–20%.

Completed industrial training performing QC operations, media preparation, equipment cleaning, and hands-on training with HPLC, UV and FTIR instruments while participating in continuous improvement activities.

MSc in Pharmaceutical Business and Technology focusing on pharmaceutical quality systems, technology transfer, and regulatory landscape; dissertation on monoclonal antibody manufacturing (India vs. Ireland).

Quality Control – wet and instrumental analysis training with hands-on experience on HPLC, GC, Karl Fischer, FTIR, UV, and pH meters; exposure to internal and customer audits.

Bachelor of Pharmacy program covering pharmaceutical analysis, organic and medicinal chemistry, microbiology, pharmaceutics, and pharmacology; dissertation on COVID-19 public health communication.