Chitvan Pandit

Background

About Chitvan Pandit

Competent, Resourceful and Analytical professional with a proven track record of innovation and development in the Pharmaceutical industry. Skilled Scientist, with an extensive experience in Pharmaceutical Research, Formulation & Development of oral solid and liquid dosage forms (powders, tablets, capsules, & syrups), Pharmacovigilance, Clinical experimentation, and Regulatory Affairs. Comprehensive understanding of ISO 9001/ ISO13485, QSR, Good Manufacturing Practices (GMP) and Microbial Processes. Passionate and inquisitive in nature with regards to medical science, API developments, and manufacturing of medicines, which leveraged into achieving multiple honours and opportunities, while still being at an entry level position. Currently associated with Dr. Reddy’s Laboratories, while being involved into complex chemical mixtures and formulation of medications. Actively participated in multiple extra-curricular projects that facilitated an opportunity to assume leadership since the academic years. This leadership attitude helped in securing a scholarship by AICTE, for GPAT 2017, AIR -146, amongst students nationwide. Attended multiple Pharma based conferences and Programmes, as a presenter, and demonstrated multiple presentations regarding various topics. Some of the presentations are as follows- A presentation on "Late phase drug product development: Values & Challenges of differentiated formulations"- at Dr. Reddy's Laboratories in 2019 - Detailed discussion on "Lipidic Nano Strategy for enhancing oral bioavailability of curcumin" at 6th ISNSCON 2018 at New Delhi - Focused Analysis on "Lifestyle Disorders: What, Why, How" at 1st IBRO/APRC Chandigarh Neuroscience Symposium (An International Scientific Event planned by UIPS, PU in 2016 Core Competencies Include: Spearheading Quality Improvement & Cost Leadership Projects Project Management & Coordination: Project Scheduling & Analysis, Scrum & Agile Methodologies, Reporting & Negotiation Involvement in Pilot Plant Design, Equipment Selection, Commissioning & Launch Scientific Expertise: Risk Assessment, QBD, DoE, Process Design & Development, Process Verification, Process Validation. Scale Up, and Tech Transfer of Semi Solid Dosage Form Technical capabilities: SAP, DocHub, S2L, Microsoft Office, Mendeley, Endnote, Research on Science Direct, PubMed, Blueprint Designing Always interested in opportunities that focus on bringing about a positive transformation in the medical industry, and contributing to overall scientific growth.