Hemant Sharma
Experienced Quality Assurance API (QA/RA) with a demonstrated history of working in the Pharmaceutical Industries as QA Site... | Rajasthan, Rajasthan, India
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Hemant Sharma’s Emails he****@ba****.com
Hemant Sharma’s Phone Numbers No phone number available.
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Hemant Sharma’s Location Rajasthan, Rajasthan, India
Hemant Sharma’s Expertise Experienced Quality Assurance API (QA/RA) with a demonstrated history of working in the Pharmaceutical Industries as QA Site Lead Skilled in cGMP compliance, ICH Guidelines, SOP, QMS, Data Integrity, Quality Risk Assessment, Total Quality Management, Lean Six Sigma Yellow Belt, Regulatory/Customer Audit interfaced like USFDA, EUGMP, MHRA, PMDA, WHO GMP, ISO 9001-2015, STADA, TAKEDA, COFPERIS, MYLAN, TEVA, ECOPHARMA, BELUPO, LUPIN, SOPHARMA, Contract Laboratory Audit, DMF Filing in CTD Format, Annual update/Query Response given to Regulatory Affairs, Preparation & Review of Quality Manual, Site Master File, Validation Master Plan, Technology Transfer Documents, SOP/cGMP related Training, Handling of QMS (Deviation, Change Control, OoS, OoT, Market Complaint, Investigation, CAPA), Peparation/Review & Approval of APQR, Vendor Qualification, Preparation/Review of Protocols/Reports of Equipment Qualification, HVAC System Validation, Water System Validation, Process Validation, Cleaning Validation, Review of BMR & COA with Analytical Records for Batch Release Activities of API/Intermediate, IPQA Activities like Sampling/Dispensing/Monitoring of Quality Records, Proficiency in SAP QM/Trackwise Software, Quality Control Documents Review, Instruments handled like Analytical Balance, pH meter, UV, FTIR, KF Titrator, Refractometer, Sieve Analyser, Leak Testing Apparatus, Bulk Density Apparatus, Viscometer,(Only awareness but not operated Instruments like HPLC, Gas Chromatography). Strong Quality Assurance professional as Problem Solving and Team Building Management with M.Sc. focused in Industrial Chemistry.
Hemant Sharma’s Current Industry Bal Pharma
Hemant
Sharma’s Prior Industry
Vvf
|
Sterling Biotech
|
Ipca Laboratories
|
Zydus
|
Torrent Pharmaceuticals
|
Bal Pharma
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Work Experience
Bal Pharma
Assistant Quality Assurance Manager
Tue Jun 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Torrent Pharmaceuticals
Executive Quality Assurance
Tue Oct 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Mar 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Zydus
Executive Quality Assurance
Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Sep 01 2013 00:00:00 GMT+0000 (Coordinated Universal Time)
Ipca Laboratories
Senior Officer Quality Assurance
Sun Feb 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2012 00:00:00 GMT+0000 (Coordinated Universal Time)
Sterling Biotech
Technical Assistant Q.C. / Q.A.
Wed Aug 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jan 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)
Vvf
Chemist Quality Control
Fri Jul 01 2005 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jul 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Hemant Sharma Email Addresses
FAQ About Hemant Sharma
-
Hemant Sharma is located at
Rajasthan, Rajasthan, India -
Hemant Sharma is a
Experienced Quality Assurance API (QA/RA) with a demonstrated history of working in the Pharmaceutical Industries as QA Site Lead Skilled in cGMP compliance, ICH Guidelines, SOP, QMS, Data Integrity, Quality Risk Assessment, Total Quality Management, Lean Six Sigma Yellow Belt, Regulatory/Customer Audit interfaced like USFDA, EUGMP, MHRA, PMDA, WHO GMP, ISO 9001-2015, STADA, TAKEDA, COFPERIS, MYLAN, TEVA, ECOPHARMA, BELUPO, LUPIN, SOPHARMA, Contract Laboratory Audit, DMF Filing in CTD Format, Annual update/Query Response given to Regulatory Affairs, Preparation & Review of Quality Manual, Site Master File, Validation Master Plan, Technology Transfer Documents, SOP/cGMP related Training, Handling of QMS (Deviation, Change Control, OoS, OoT, Market Complaint, Investigation, CAPA), Peparation/Review & Approval of APQR, Vendor Qualification, Preparation/Review of Protocols/Reports of Equipment Qualification, HVAC System Validation, Water System Validation, Process Validation, Cleaning Validation, Review of BMR & COA with Analytical Records for Batch Release Activities of API/Intermediate, IPQA Activities like Sampling/Dispensing/Monitoring of Quality Records, Proficiency in SAP QM/Trackwise Software, Quality Control Documents Review, Instruments handled like Analytical Balance, pH meter, UV, FTIR, KF Titrator, Refractometer, Sieve Analyser, Leak Testing Apparatus, Bulk Density Apparatus, Viscometer,(Only awareness but not operated Instruments like HPLC, Gas Chromatography). Strong Quality Assurance professional as Problem Solving and Team Building Management with M.Sc. focused in Industrial Chemistry. Bal Pharma -
Hemant Sharma currently works in the
Bal Pharma -
Hemant Sharma specializes in
Experienced Quality Assurance API (QA/RA) with a demonstrated history of working in the Pharmaceutical Industries as QA Site Lead Skilled in cGMP compliance, ICH Guidelines, SOP, QMS, Data Integrity, Quality Risk Assessment, Total Quality Management, Lean Six Sigma Yellow Belt, Regulatory/Customer Audit interfaced like USFDA, EUGMP, MHRA, PMDA, WHO GMP, ISO 9001-2015, STADA, TAKEDA, COFPERIS, MYLAN, TEVA, ECOPHARMA, BELUPO, LUPIN, SOPHARMA, Contract Laboratory Audit, DMF Filing in CTD Format, Annual update/Query Response given to Regulatory Affairs, Preparation & Review of Quality Manual, Site Master File, Validation Master Plan, Technology Transfer Documents, SOP/cGMP related Training, Handling of QMS (Deviation, Change Control, OoS, OoT, Market Complaint, Investigation, CAPA), Peparation/Review & Approval of APQR, Vendor Qualification, Preparation/Review of Protocols/Reports of Equipment Qualification, HVAC System Validation, Water System Validation, Process Validation, Cleaning Validation, Review of BMR & COA with Analytical Records for Batch Release Activities of API/Intermediate, IPQA Activities like Sampling/Dispensing/Monitoring of Quality Records, Proficiency in SAP QM/Trackwise Software, Quality Control Documents Review, Instruments handled like Analytical Balance, pH meter, UV, FTIR, KF Titrator, Refractometer, Sieve Analyser, Leak Testing Apparatus, Bulk Density Apparatus, Viscometer,(Only awareness but not operated Instruments like HPLC, Gas Chromatography). Strong Quality Assurance professional as Problem Solving and Team Building Management with M.Sc. focused in Industrial Chemistry. -
Hemant Sharma speaks the following languages:
No languages available. -
Hemant Sharma has prior experience in the following industries:
Torrent Pharmaceuticals , Zydus , Ipca Laboratories , Sterling Biotech , Vvf -
Hemant Sharma has the following professional experience:
Bal Pharma , Torrent Pharmaceuticals , Zydus , Ipca Laboratories , Sterling Biotech , Vvf . -
You can view Hemant Sharma’s
LinkedIn profile at LinkedIn URL. -
Hemant Sharma’s work email addresses are
[email protected] . -
Hemant Sharma works at
Bal Pharma
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