Eli Lilly and Company May 2013 - May 2013
Director, Global Quality Auditing and Compliance at Eli Lilly and Company
Ipr Pharmaceuticals Inc. 1991 - 1996
Regulatory Affairs Supervisor
Education:
University of Puerto Rico - Cayey
Bachelors, Bachelor of Science, Chemistry
Skills:
Fda Gmp Regulatory Affairs Pharmaceutical Industry Quality Auditing Change Control Capa Gxp 21 Cfr Part 11 Validation Quality System Quality Assurance Computer System Validation Sop Pharmacovigilance Quality Control Manufacturing Technology Transfer Regulatory Submissions Clinical Trials Biopharmaceuticals Aseptic Processing Cleaning Validation Quality Management Gamp Regulatory Requirements Pharmaceutics Lims Clinical Development Analytical Chemistry Fda Gmp Drug Development Hplc Trackwise Cgmp Practices Chromatography Deviations Cro