VEDANT ANIL JAGTAP
Nashik
Summary
B.Pharm final year student at RG Sapkal Institute of Pharmacy, with hands-on expertise in cGMP-compliant production, QC/QA documentation, SOP adherence, and regulatory awareness (Schedule M, ICH guidelines). Currently authoring research on phytofabricated ZnO nanoparticles with antifungal applications. Seeking a QC/QA or production role where quality is not an afterthought.
Overview
1
1
year of professional experience
5
5
years of post-secondary education
Work History
Lead Researcher
RG Sapkal Institute of Pharmacy
08.2025 - 06.2026
- Synthesised and characterised ZnO nanoparticles with confirmed antifungal activity, demonstrating a synergistic inhibition zone greater than the standard drug control, by optimising green synthesis parameters (extract concentration, pH, temperature) and evaluating via disc diffusion method.
- Ensured reproducibility and scientific validity across triplicate runs by applying UV-Vis spectroscopy for nanoparticle confirmation and adhering to ICH Q2(R1) analytical method validation principles.
- Delivered a structured research report aligned to pharmaceutical R&D dossier format, covering synthesis, characterization, and efficacy sections in full.
Production Intern
Shriniwasa Ayurvedic Pvt Ltd
06.2025 - 07.2025
- Supported cGMP-compliant production runs with zero batch rejections across 3 monitored batches by following SOPs rigorously, performing in-process quality checks at each critical control point, and maintaining accurate batch records.
- Reduced documentation errors in daily production logs by flagging 2 discrepancies before sign-off, cross-verifying batch manufacturing records (BMRs) against dispensed quantities using MS Excel tracking sheets.
- Shadowed QA team during internal line clearance audits and equipment cleaning verification to understand Schedule M compliance requirements across all stages of ayurvedic oral dosage form production.
Education
B.Pharmacy - QC, QA, Regulatory Affairs Knowledge
RG Sapkal Institute of Pharmacy
Nashik , India 01.2023 - 06.2026
Class XII - Biological Sciences
Gyan Ganga English Medium High School
Vapi, India 04.2021 - 01.2022
Class X -
Gyan Ganga English Medium High School
Vapi, India 04.2019 - 01.2020
Skills
- Research Documentation
- Quality Assurance
- Regulatory Compliance
- CGMP
- SOP Writing
- In-process QC
- ICH Guidelines
- Microbial Testing
- UV-Vis Spectroscopy
- Titration
- Material Analysis
- Documentation & Reporting
- MS Excel
- MS Office
- Documentation & Reporting
Accomplishments
- Department topper in B.Pharmacy at RG Sapkal Institute of Pharmacy (Top 3 in class, CGPA 8.25).
- Top 3 in class throughout school — scored 89.91% in Class X and 71.95% in Class XII (Gujarat Board).
Languages
English, Read, Write, Speak
Projects
Lead Researcher, RG Sapkal Institute of Pharmacy, 08/01/25, 06/30/26, Phytofabrication & Evaluation of Zinc Oxide Nanoparticles using Vitex Negundo Seed Extract, Synthesised and characterised ZnO nanoparticles with confirmed antifungal activity, demonstrating a synergistic inhibition zone greater than the standard drug control, by optimising green synthesis parameters (extract concentration, pH, temperature) and evaluating via disc diffusion method., Ensured reproducibility and scientific validity across triplicate runs with consistent results by applying UV-Vis spectroscopy for nanoparticle confirmation and following ICH Q2(R1) analytical method validation principles., Delivered a structured research report aligned to pharmaceutical R&D dossier format, covering synthesis, characterisation, and efficacy sections in full.
Core Skills
cGMP, SOP Writing, BMR / BPR, In-process QC, Schedule M, ICH Guidelines, UV-Vis Spectroscopy, Disc Diffusion, Titration, ZnO Nanoparticle Characterisation, MS Excel, MS Office, Documentation & Reporting
Internship
Production Intern, Shriniwasa Ayurvedic Pvt Ltd, 06/01/25, 07/31/25, Supported cGMP-compliant production runs with zero batch rejections across 3 monitored batches by following SOPs rigorously, performing in-process quality checks at each critical control point, and maintaining accurate batch records., Reduced documentation errors in daily production logs by flagging 2 discrepancies before sign-off, cross-verifying batch manufacturing records (BMRs) against dispensed quantities using MS Excel tracking sheets., Gained hands-on exposure to Schedule M compliance requirements across all stages of ayurvedic oral dosage form production by shadowing the QA team during internal line clearance audits and equipment cleaning verification.
Languages
English
Advanced
C1
Hindi
Proficient
C2
Marathi
Proficient
C2
Timeline
Lead Researcher
RG Sapkal Institute of Pharmacy
08.2025 - 06.2026
Production Intern
Shriniwasa Ayurvedic Pvt Ltd
06.2025 - 07.2025
B.Pharmacy - QC, QA, Regulatory Affairs Knowledge
RG Sapkal Institute of Pharmacy
01.2023 - 06.2026
Class XII - Biological Sciences
Gyan Ganga English Medium High School
04.2021 - 01.2022
Class X -
Gyan Ganga English Medium High School
04.2019 - 01.2020