M.Pharm
I am a Pharmaceutical Chemistry R&D professional with core expertise in Organic Synthesis and Analytical Chemistry, supported by extensive hands-on experience in research-driven laboratory environments. My primary focus involves the design and synthesis of organic molecules, chromatographic method development, impurity profiling, and advanced analytical characterization using GC, HPLC, NMR, MS, GC–MS, LC–MS, IR, and UV-based techniques.
I possess strong practical exposure to synthesis-oriented research, structural elucidation, and analytical method optimization conducted with scientific rigor and adherence to global quality standards. I also have operational experience in handling and troubleshooting analytical instrumentation such as GC and HPLC systems. In addition, I maintain working knowledge of Regulatory Affairs principles, ensuring that research and analytical processes align with international pharmaceutical regulatory frameworks and compliance requirements.
Beyond laboratory research, I have published peer-reviewed scientific research papers, demonstrating my proficiency in scientific writing, data interpretation, and research communication. I also actively engage in delivering lectures and knowledge-sharing sessions on Organic Synthesis, Analytical Chemistry, and personal development skills, reflecting my ability to translate complex scientific concepts into clear and impactful communication.
Advanced Organic Synthesis
Heterocyclic Compound Design & Development
Reaction Mechanism Elucidation
Structure–Activity Relationship (SAR) Studies
Chiral Molecule Synthesis & Separation
Green Chemistry Approaches in API Development
Advanced Chromatographic Method Development
Analytical Method Optimization & Troubleshooting
Structure Elucidation Using Spectroscopic Techniques
Impurity Profiling & Degradation Pathway Studies
Stability-Indicating Method Development
Trace-Level Quantification & Analytical Sensitivity Enhancement
CMC (Chemistry, Manufacturing & Controls) Documentation
Regulatory Science & Compliance Strategy
Quality by Design (QbD) Principles
ICH Guideline Implementation
Data Integrity & GMP Compliance
🔬 Analytical Techniques
Gas Chromatography (GC-FID)
GC–MS (Qualitative & Quantitative Analysis)
Headspace GC for Residual Solvents
High-Performance Liquid Chromatography (HPLC)
Reverse Phase & Normal Phase Chromatography
Gradient & Isocratic Method Development
Nuclear Magnetic Resonance (¹H & ¹³C NMR)
Mass Spectrometry (MS)
LC–MS
Infrared Spectroscopy (IR)
UV–Visible Spectroscopy
ICH Q2(R1) Method Validation
System Suitability & Calibration
Forced Degradation Studies
Stability Testing as per ICH Guidelines
USP <467> Residual Solvent Analysis
🧪 Technical Expertise
Advanced Chromatographic Method Development
Assay & Related Substance Analysis
Impurity Identification & Profiling
Residual Solvent Quantification
Method Validation & Transfer
Instrument Handling & Troubleshooting (GC, HPLC)
Empower & LabSolutions Software
Analytical Data Interpretation
Regulatory Documentation & CMC Module Support
GLP & GMP-Compliant Laboratory Practices
💪 Core Strengths & Skills
Strong foundation in Organic Reaction Chemistry
Deep understanding of Chromatogram Interpretation
Analytical Problem-Solving & Root Cause Investigation
Experimental Design & Optimization
Scientific Writing & Research Publication Experience
Published Peer-Reviewed Research Papers
Technical Presentation & Lecture Delivery
Ability to Explain Complex Scientific Concepts Clearly
Scientific Documentation & Report Preparation
Cross-Functional Communication (R&D & Regulatory Teams)
Research-Oriented Mindset
High Attention to Detail
Adaptability to Advanced Technologies
Continuous Learning Attitude
Leadership & Knowledge-Sharing Initiative
💼 Professional Experience
Chromatographic method development and optimization
Assay determination and related substance analysis
Impurity profiling & residual solvent analysis
Stability-indicating method development
Analytical method validation as per ICH guidelines
GC instrumentation operation, calibration & troubleshooting
Regulatory documentation support (CMC sections)
Data review, interpretation, and compliance verification
