Position:
Validation Consultant at Pharmaceutical
Work:
Pharmaceutical
since Apr 2013
-
Validation Consultant
Sandoz
- Broomfield CO Mar 2011 - Mar 2013
-
Manager Finished Dosage/ Packaging Operations
BOEHRINGER INGELHEIM CHEMICALS, Inc
Aug 2009 - Mar 2011
-
Complaince Analyst II
Boehringer Ingelheim
- Petersburg Virginia Aug 2008 - Aug 2009
-
Production Supervisor
Pfizer
Feb 2007 - May 2008
-
Shift Team Leader
Teva Pharmaceuticals
Jun 2004 - Nov 2006
-
Sr. Supervisor Granulation
Schering Plough
May 2000 - Jun 2004
-
Compression Supervisor
Searle
Feb 1997 - May 2000
-
Process Flow Assurer
Wesley Jessen
Feb 1990 - May 1997
-
Microbiologist, Validation Specialist, Production Supervisor
Alejandro Buitrago Hospital
Aug 1988 - Feb 1990
-
Medical Technologist
Education:
Pontifica Universidad Catolica de Puerto Rico 1986 - 1987
MT Certificate, Medical Technologist
Universidad de Puerto Rico 1981 - 1986
BS, Biology, Chemistry
Skills:
GMP, Root Cause Analysis, Pharmaceutics, Process Improvement, Pharmaceutical Industry, Cleaning Validation, 21 CFR Part 11, Validation, Chemistry, Sop, Lean Manufacturing, Quality Auditing, CAPA, V&V, Manufacturing, Regulatory Affairs, Quality System, Biotechnology, FDA, Technology Transfer, Change Control