Rutuja Jadhav

M.Pharm (Pharmaceutics) postgraduate with a foundation in drug safety, pharmacovigilance, clinical research, and medical writing. Know MedDRA coding, ICH E2A/E2B/E2C safety guidelines, literature analysis, and pharmacological concepts developed through academic research and M.Pharm dissertation work. CSIR-UGC NET qualified with hands-on expertise in QbD-based pharmaceutical research, clinical trial processes, and cross-functional collaboration in regulated environments.

Adept at medical literature review, adverse event documentation, signal detection concepts, and translating complex scientific data into clear regulatory narratives.

QA/QC & Manufacturing Intern at Nulife Pharmaceuticals Pvt. Ltd. (2025-02 – 2025-03)

• Assisted in batch record review and GMP documentation, identifying documentation gaps under QA/QC supervision
• Performed dissolution testing and UV analysis as per SOPs, supporting QC data generation
• Gained exposure to GMP documentation practices, including BMR, deviation handling, and change control systems
• Observed end-to-end manufacturing processes, understanding workflow from dispensing to packaging

M.Pharm in Pharmaceutics – Smt. Kashibai Navale College of Pharmacy, Pune (SPPU) (2023 – 2025-11)

B.Pharm – Government College of Pharmacy, Karad (2023)

H.S.C. – Laxmanrao Kirloskar Junior College, Palus (2019)

S.S.C. – Swami Ramanand Vidyalaya, Ramanand Nagar (2017)