Hemlata Shinde

Hemlata Shinde

Associate Director @ Bristol Myers Squibb

About Hemlata Shinde

Hemlata Shinde is an Associate Director at Bristol-Myers Squibb in New Jersey, with extensive experience in IT Quality Assurance within the pharmaceuticals industry.

Current Position at Bristol-Myers Squibb

Hemlata Shinde currently serves as an Associate Director at Bristol-Myers Squibb in New Jersey. She began her current role in November 2018, bringing with her extensive experience in IT Quality Assurance within the pharmaceuticals industry.

Past Roles in Pharmaceuticals and Airlines

Hemlata Shinde has held numerous positions over her career, reflecting her deep expertise in quality assurance and validation. Prior to her current role, she was the Compliance and Validation Lead at Johnson & Johnson for two years. She also worked at JetBlue Airways as a Sr. Quality/Validation Analyst for six months, and at Canon U.S.A Inc as a Sr. Quality Analyst for two years. Earlier in her career, she served as a Sr. Quality Assurance Professional at Sitel for three years.

Long Tenure with Bristol-Myers Squibb

Before becoming an Associate Director at Bristol-Myers Squibb, Hemlata Shinde had a strong eight-year tenure with the company. From 2009 to 2016, she worked as an SAP Validation Specialist, a role in which she honed her skills in managing change control processes and ensuring compliance with GMP standards.

Educational Background

Hemlata Shinde's academic qualifications include multiple degrees from reputable institutions. She earned a Master's in Management and a Master of Science from the New York Institute of Technology between 2006 and 2008. Additionally, she holds a Bachelor of Commerce and a Master of Commerce from Mumbai University. She also holds a Bachelor of Commerce from NIIT Institute.

Expertise in IT Quality Assurance

Hemlata Shinde's career is marked by extensive experience in IT Quality Assurance within the pharmaceuticals industry. She is particularly skilled in managing change control processes and ensuring compliance with GMP standards. Her strong background in document management and validation has made her a valuable asset in her various roles.

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