Qa/qc Head
Hemant Prajapati
Scientific Writing
About me
Scientific documentation professional with over 4.5 years of experience in pharmaceutical Quality Assurance and regulatory environments. Expert in converting complex analytical data into structured, regulator-ready documentation while ensuring strict GMP and GLP compliance. Proven track record in SOP authoring, deviation management, and audit support, backed by a Master’s degree in Chemistry with a 9.25 CGPA
Interests: Organic & Heterocyclic Synthesis: Specialized in the synthesis and optimization of bioactive molecules, specifically focusing on the conversion of chalcones to pyrazoles. Methodology Development: Interested in reaction monitoring, yield optimization, and refining laboratory techniques to improve chemical purity. Analytical Interpretation: Deep interest in the structural characterization of compounds and the analytical interpretation of experimental data. Regulatory & Quality Science: Researching the integration of GMP-compliant documentation with scientific reporting to ensure data traceability and integrity. Green Chemistry: Exploring sustainable chemical processes and efficient waste management in pharmaceutical manufacturing environments.
My Services
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