
Timeline
About me
Deputy Manager at Cipla API R&D
Education
Prof ramkrishna more arts,commerce & science college, akurdi, pune 44
2003 - 2006B.sc chemistry first class with distinctionModern education society's nowrosjee wadia college arts, science, pune 01
2006 - 2008Master in science m.sc analytical chemistry first class
Experience
Glenmark pharmaceuticals
May 2008 - May 2011Research associateBioanalytical method development, validation and in blood, Plasma by LC-MS/MS.
Accutest research laboratories (i) pvt. ltd.
May 2011 - Jul 2014Research associateBioanalytical method development and method validation drug Product in Blood, serum and Plasma by using LC-MS/MS
Emcure pharmaceuticals limited
Jul 2014 - Apr 2016Research officer1.Impurity Profiling, Identification of unknown impurity and Quantification of Genotoxic impurity By LC-MS/MS.2.Method development and Validation of Elemental impurities by ICP-MS and ICP-OES.3.troubleshooting and maintenance of Instrument such as LC-MS, ICP-MS, ICP-OES, HPLC and XRD.
Cipla
Apr 2016 - now1. Monitoring the activity of Elemental Impurities for Drug Substance and Drug Product by Using ICP-MS and ICP-OES.2. Co-ordinate with Regulatory and Synthetic team for Elemental Impurities and Risk assessments for Final API.Also Selection of Element and Limit as per ICH Q3D.3. Method Development and Validation of Elemental Impurities as per ICH Q3D by Using ICP-MS and ICP-OES.4 Familier with Method transfer activity at Quality control department and guide with respective department.5. Guide the team member for Method development and Validation activity.6. Review the Validation Protocol, Data sheet and Method Validation Report as per GLP compliance.7. Impurity profiling for Raw material, intermediate and Final API by LC-MS and MS-MS with interpretation.8. Identification of unknown impurity in Intermediate and final API by LC-MS.9. Method Development and Optimization of MRM (product ion) MS/MS for API molecule, Impurities.Validate the method as per Validation Protocol of various methods.10. Development of LCMS compatible analytical method using volatile buffers as an alternative for non-volatile phosphate buffer method.11.Familiar with Calibration of Instrument and review report such as LC-MS. HPLC, ICP-MS and ICP-OES.12.Determination of Elemental composition such as C,H,N,S,O &Cl of final API by using CHNSO Analyzer.13 Familier with calibration, maintainace and troubleshooting of CHNSO Analyzer. Show less
Deputy Manager
Jul 2022 - nowAssistant Manager
Apr 2016 - Aug 2022
Licenses & Certifications
Lean six sigma yellow belt certification
6sigmastudy - the global certification body for six sigma certificationsApr 2021Six sigma and lean:foundetions and principles
SkillsoftScrum fundamentals certified (sfc)
Scrumstudy - accreditation body for scrum and agileApr 2021
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