Siddhanta Ghosh

M.Pharm (Pharmaceutical Analysis) postgraduate with hands-on experience in analytical method development, validation, and characterization of drug candidates using RP-HPLC, UV-Visible Spectrophotometry, and FT-IR. Trained across QC and QA functions at generic drug manufacturing units, with working knowledge of GLP, GMP, ICH guidelines, and USFDA regulatory requirements. Research experience in synthesis, characterization, and antimicrobial evaluation of cinnamamide/cinnamic acid derivatives, supported by SAR analysis, QSAR, and molecular docking studies.

Seeking to contribute analytical rigor and research discipline to a QC, QA, or AR&D role in the pharmaceutical industry.

Industrial Training — QC & QA - DCI Pharmaceuticals Pvt. Ltd. - Goa

• Gained exposure to routine QC testing workflows and QA departmental practices in a generic drug manufacturing environment

Industrial Training — Production - Dr. Sain's Laboratories - Kolkata, WB

• Observed production unit operations and GMP-compliant manufacturing practices

Technical Training — QA & QC - Sura Pharma Labs - Hyderabad

• Trained in QA and QC departmental procedures, including documentation practices and quality checks

Hospital Training (1 month) - Primary Health Centre - Baital, Bankura, WB

• Gained clinical/pharmacy practice exposure in a primary healthcare setting

M.Pharm - Pharmaceutical Analysis - Dr. B.C. Roy College of Pharmacy and Allied Health Sciences, Durgapur (MAKAUT) (2026)

B.Pharm - Sanaka Educational Trust's Group of Institution, Durgapur (MAKAUT) (2023)

Higher Secondary - Baital Gopeaswar Pal Vidyapith (H.S.), WBCHSE (2019)

Secondary - Baital Gopeaswar Pal Vidyapith (H.S.), WBBSE (2017)