Experience

iMEDGlobal Corporation

• United States
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Regulatory Affairs Executive

  • Apr 2016 - Present

  IDMP-CMC EMEA CDPM IDMP-CMC EMEA CDPM



Freyr Solutions

• United States
• IT Services and IT Consulting
• 700 & Above Employee

• Regulatory Associate

  • Dec 2015 - Apr 2016

  Regulatory Intelligence Services Regulatory Intelligence Services



Virchow Biotech Pvt Ltd - India

• India
• Airlines and Aviation
• 200 - 300 Employee

• Regulatory Affairs Executive

  • Mar 2015 - Sep 2015

  510k filings, Dossier filing (module 3) 510k filings, Dossier filing (module 3)



Shiva's Farma Casa (P) Ltd.

• Secunderabad

• Technical Executive

  • Dec 2013 - Feb 2015

  Dossier compilation , review and handling of queries for LATAM countries. To appraise the knowledge on the latest regulatory requirements of LATAM countries and share with the group. Preparing the Checklist for required Documents according to the country guidelinesDossier Review, Handling of Queries, Plant visits Dossier compilation , review and handling of queries for LATAM countries. To appraise the knowledge on the latest regulatory requirements of LATAM countries and share with the group. Preparing the Checklist for required Documents according to the country guidelinesDossier Review, Handling of Queries, Plant visits



NATCO PHARMA LTD

• Hyderābād Area, India

• Project Trainee

  • Aug 2012 - Jan 2013

  Dossier compilation (ACTD/CTD), review and handling of queries for ASEAN and LATAM countries. To appraise the knowledge on the latest regulatory requirements of ASEAN and LATAM countries and share with the group. Preparing the Checklist for required Documents according to the country guidelines. Interacting with all concerned departments (Production, QA, QC, R&D and projects) concerning the Regulatory submissions and Compliance. Dossier compilation (ACTD/CTD), review and handling of queries for ASEAN and LATAM countries. To appraise the knowledge on the latest regulatory requirements of ASEAN and LATAM countries and share with the group. Preparing the Checklist for required Documents according to the country guidelines. Interacting with all concerned departments (Production, QA, QC, R&D and projects) concerning the Regulatory submissions and Compliance.



Dr. Reddy's Laboratories

• India
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Project Trainee

  • Jun 2012 - Jul 2012

  Exposure to different departments in Pharmaceutical Industry. Quality Assurance Department - worked on Batch manufacturing records Exposure to different departments in Pharmaceutical Industry. Quality Assurance Department - worked on Batch manufacturing records