Sharvari Borkar sharvari.borkar@gsk.com & | CMC leader with proven track record of successfully leading global matrix cross functional teams in developing and implementing global regulatory strategies. Possess an unique combination of strong technical skills, project management experience and regulatory expertise. Deep functional knowledge of Pharmaceutical Sciences, clear understanding and hands-on experience in drug development, manufacturing and process improvements Specialties: • CMC Strategy & Risk Management • ICH Q12 • Agency Interactions • Quality by Design (QbD) • Lean Six Sigma • Product / Process Scale Up • 3rd Party Technology Transfers • Formulations Development • Process Validations • cGMP

Sharvari Borkar

CMC leader with proven track record of successfully leading global matrix cross functional teams in developing and implementing...

Greater Philadelphia, Greater Philadelphia, United States

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Sharvari Borkar’s Emails [email protected]

Sharvari Borkar’s Phone Numbers No phone number available.

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Sharvari Borkar’s Location Greater Philadelphia, Greater Philadelphia, United States

Sharvari Borkar’s Expertise CMC leader with proven track record of successfully leading global matrix cross functional teams in developing and implementing global regulatory strategies. Possess an unique combination of strong technical skills, project management experience and regulatory expertise. Deep functional knowledge of Pharmaceutical Sciences, clear understanding and hands-on experience in drug development, manufacturing and process improvements Specialties: • CMC Strategy & Risk Management • ICH Q12 • Agency Interactions • Quality by Design (QbD) • Lean Six Sigma • Product / Process Scale Up • 3rd Party Technology Transfers • Formulations Development • Process Validations • cGMP

Sharvari Borkar’s Current Industry Bristol Myers Squibb

Sharvari Borkar’s Prior Industry
Eli Lilly | Merck | Gsk | Bristol Myers Squibb

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Work Experience

Bristol Myers Squibb

Associate Director, Global Regulatory CMC

Tue Feb 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Gsk

CMC Global Regulatory Manager

Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Feb 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Gsk

Formulation Scientist

Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Dec 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time)

Merck

Product Development Engineer

Wed Apr 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jan 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)

Eli Lilly

Research Scientist

Tue Jan 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Mar 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)

Eli Lilly

Manufacturing Scientist

Sat Mar 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Dec 01 2007 00:00:00 GMT+0000 (Coordinated Universal Time)

Eli Lilly

Associate Formulations Scientist - Animal Health Research

Sun Jul 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Feb 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time)

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FAQ About Sharvari Borkar

Sharvari Borkar is located at
Greater Philadelphia, Greater Philadelphia, United States

Sharvari Borkar is a
CMC leader with proven track record of successfully leading global matrix cross functional teams in developing and implementing global regulatory strategies. Possess an unique combination of strong technical skills, project management experience and regulatory expertise. Deep functional knowledge of Pharmaceutical Sciences, clear understanding and hands-on experience in drug development, manufacturing and process improvements Specialties: • CMC Strategy & Risk Management • ICH Q12 • Agency Interactions • Quality by Design (QbD) • Lean Six Sigma • Product / Process Scale Up • 3rd Party Technology Transfers • Formulations Development • Process Validations • cGMP Bristol Myers Squibb

Sharvari Borkar currently works in the
Bristol Myers Squibb

Sharvari Borkar specializes in
CMC leader with proven track record of successfully leading global matrix cross functional teams in developing and implementing global regulatory strategies. Possess an unique combination of strong technical skills, project management experience and regulatory expertise. Deep functional knowledge of Pharmaceutical Sciences, clear understanding and hands-on experience in drug development, manufacturing and process improvements Specialties: • CMC Strategy & Risk Management • ICH Q12 • Agency Interactions • Quality by Design (QbD) • Lean Six Sigma • Product / Process Scale Up • 3rd Party Technology Transfers • Formulations Development • Process Validations • cGMP