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Cindy Marin Location
Carmel, IN, US
Cindy Marin Work
Director, Global Quality Auditing and Compliance (Medical, Patient Safety, Regulatory) @ Eli Lilly and Company (May 2013 - Present)
Director, Global Quality Auditing and Compliance (Commercial Manufacturing, Drug Safety, Regulatory) @ Eli Lilly and Company (November 2010 - May 2013)
Director, Global Quality Compliance @ Eli Lilly and Company (September 2004 - November 2010)
Site Quality Leader, Indianapolis Dry Products Operations @ Eli Lilly and Company (September 2002 - September 2004)
Site Quality Leader, Lilly del Caribe PR01 @ Eli Lilly and Company (January 1999 - August 2002)
Regulatory Affairs Supervisor, Lilly del Caribe @ Eli Lilly and Company (June 1996 - December 1998)
Regulatory Affairs Supervisor @
Cindy Marin Education
University of Puerto Rico
Bachelor of Science (BSc) (Chemistry)
Cindy Marin Skills
GMP
CAPA
21 CFR Part 11
FDA
Pharmaceutical Industry
GxP
Change Control
Computer System Validation
Validation
Sop
Quality System
Regulatory Affairs
Aseptic Processing
Cleaning Validation
Quality Auditing
GAMP
Clinical Trials
Manufacturing
Regulatory Submissions
Quality Control
Pharmacovigilance
Quality Management
Regulatory Requirements
Analytical Chemistry
FDA GMP
Drug Development
Biopharmaceuticals
Pharmaceutics
HPLC
Technology Transfer
Trackwise
LIMS
cGMP practices
Clinical Development
Deviations
Chromatography
Quality Assurance
CRO
Public Relations
Social Media
Cindy Marin Summary
Cindy Marin, based in Carmel, IN, US, is currently a Director, Global Quality Auditing and Compliance (Medical, Patient Safety, Regulatory) at Eli Lilly and Company. Cindy Marin brings experience from previous roles at Eli Lilly and Company. Cindy Marin holds a Bachelor of Science (BSc) in Chemistry @ University of Puerto Rico. With a robust skill set that includes GMP, CAPA, 21 CFR Part 11, FDA, Pharmaceutical Industry and more. Cindy Marin has 3 emails and 2 mobile phone numbers on RocketReach.
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