Experience

Steriscience

• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Senior Team leader

  • Apr 2023 - Present

  Analytical Quality Assurance

• Support Team Lead

  • Dec 2021 - Jul 2023

  Handling laboratory QMS, OOS, OOT,Deviations,Change controls,CAPAs,handling software's like trackwise,SAP,LIMS EDMS, Review of analytical records generated in the laboratory, Review of qualification records for the laboratory instruments through evalgenesis version 4.1, Anytime audit readiness for any FDA inspections



Viatris

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Team Leader

  • Mar 2021 - Oct 2022



Syngene International Limited

• India
• Research Services
• 700 & Above Employee

• Senior Executive

  • Aug 2015 - Oct 2022

  Working as Analytical Reviewer in the quality Assurance Department Working as Analytical Reviewer in the quality Assurance Department



BeloorBayir Biotech Ltd.

• Tumkur

• QA Executive

  • May 2014 - Oct 2022

  QA Documentation, Maintaining QMS, Handling of CAPA,Change Control, Deviation,Market Complaints. QA Documentation, Maintaining QMS, Handling of CAPA,Change Control, Deviation,Market Complaints.



Mylan

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Associate

  • Jan 2012 - May 2014

  Handling of HPLC,UV and IR for the SFG,Inprocess and Finished Goods.Performing Physical Parameters. Handling of HPLC,UV and IR for the SFG,Inprocess and Finished Goods.Performing Physical Parameters.



Juggat Pharma

• India
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• QA Chemist

  • Jun 2010 - Dec 2011

  In-Process Checks,Issuing of BMRs and BPRs,Preparation of BMRs, Attending of Trainings. In-Process Checks,Issuing of BMRs and BPRs,Preparation of BMRs, Attending of Trainings.