Pavan Kumar Dappili

Analytical Scientist Iii @Piramal Pharma Solutions

Lexington, KY, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Aug 2021 — Present

Analytical Scientist Iii @Piramal Pharma Solutions

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Lexington, KY, US

EDUCATION

N/A

Georgia State University

Master of Science - MS

2006 — 2010

Bapuji pharmacy college, Davangere, Karnataka

Bachelor of Pharmacy (B. Pharm), Pharmacy

2003 — 2005

Board of Intermediate Education, Hyderabad

Biology, Physics, Chemistry

2011 — 2013

National Institute of Pharmaceutical Education and Research (NIPER) ,SAS NAGAR , Mohali

M.S. (Pharm.), Department of Pharmaceutical analysis

2002 — 2003

Board of Secondary Education, Hyderabad

S. S. C.

SKILLS

GlpBiochemistryCharacterizationParticle Size AnalysisUv/VisFormulationPharmaceutical IndustryPharmacologyRegulatory AffairsLifesciencesHigh-Performance Liquid Chromatography (Hplc)GmpForced Degradation StudiesPharmacokineticsIn VivoBioanalytical Method DevelopmentChromatographyLc-MsQuality SystemLife SciencesDissolutionDrug DesignStandard Operating Procedure (Sop)PharmaceuticsDrug DiscoveryAnalytical Method ValidationNmrPharmaceutical ResearchValidationMass SpectrometryMedicinal ChemistryHplcAnalytical Methods DevelopmentAnalytical ChemistryLiquid Chromatography-Mass Spectrometry (Lc-Ms)ChemistryResearch and Development (R&D)Dissolution Testing

ABOUT PAVAN KUMAR DAPPILI

An industrial experienced pharma professional having strong expertise in analytical chemistry- Having around 6 years of industrial experience for generic regulated markets (Formulations) and 7 years of experimental research experience- Hands-on experience with working, developing methods, and troubleshooting of modern analytical instruments like HPLC, LC-MS, Dissolution tester, KF- Strong oral, written, and presentation skills and good team playerSpecialties: A. Industrial experience- Handling HPLC - with detectors like Mass Spectrometry, UV-Vis, and Corona CAD- Experience in handling GC analysis- Analytical method development and validation for tests like Assay, Related Substances, Dissolution, etc- Solubility studies (Intrinsic dissolution and Saturation solubility)- Excipients compatibility study - required in supporting the product development- Drug product stability testing and purity Profiling- Routine analysis for Assay, Dissolution, Related Substances, Content uniformity, and Water content- Experienced in converting HPLC method to Mass spectrometry compatible method for LC-MS analysis- Experienced in handling the query resolution and providing the support needed for timely response to the queryB. Bioanalytical experience- Drug Metabolism and Metabolite identification atudy- LC-MS quantification of drug and it\'s metabolites in plasmaC. Academic experience- Have experience in carrying out research involving thermoanalytical techniques like DSC, TGA, DVS

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