Luis V Feliciano is a high-skilled expert, working in Teva Pharmaceuticals as a Site General Manager from 2019. Luis V Feliciano has earned professional experience in more than 13 positions at various companies. Luis V Feliciano went to the University of Puerto Rico and was studying there. Fairfield, New Jersey is the city, where this expert was known to live. Luis V Feliciano's contacts are accessed through SoftwareOfficial on demand.
Name variants:
Luis Feliciano
Last updated Jun 03, 2024
Contact Information
Last Update
Jul 1, 2022
Email
lu**@yahoo.com
Location
Fairfield, NJ
Company
Teva Pharmaceuticals
Workplace
Site General Manager
Work History
Associate Director, Pharmaceutical Technology
100 Enterprise Dr, Rockaway, NJ 07866
Warner Chilcott is a leading mid-size specialty pharmaceutical company focused on developing, manufacturing and marketing and selling branded prescription pharmaceutical products in women's ...
Aug 2013 — Dec 2013
Senior Consultant, Pharmaceutical Manufacturing
705 Front St, Toledo, OH 43605
Jan 2013 — Aug 2013
Director, Manufacturing
5320 Legacy Dr, Plano, TX 75024
Managed $2M budget, third party resources, process development and technology transfer activities pertaining to manufacture of late stage clinical through commercial supplies of drug product...
Aug 2011 — Dec 2012
Senior Scientist Ii
Directly responsible for the execution of process support, process development and technology transfer projects in a solid oral dosage operation. Completed engineering and feasibility batche...
May 2009 — Jul 2011
Technology Associate Director
New York, NY
Managed a department responsible for operations support, process validation, cleaning validation and equipment qualification in a solid oral dosage operation. Led team to complete equipment ...
Jan 2007 — Apr 2008
Pharmaceutical Technology Director
Managed a department responsible for operations support, validation (process & cleaning validation) and technology transfer, in a solid oral dosage operation. Each group had a manager with ...
Aug 2003 — Dec 2006
Technical Services Director
Managed a department responsible for validation (process & cleaning validation) and equipment qualification in a solid oral dosage manufacturing operation. Each group had a manager with 3-5...
Aug 2001 — Aug 2003
Manufacturing Operations Manager
Illinois
Managed manufacturing operations and process support engineering, with budget of $20M to $30M; 70 products and over 120 employees plus 5 section managers. Consistently met operational object...
2000 — 2001
Technical Services Manager
Illinois
Managed group responsible for process & cleaning validation, equipment qualification, computer validation and training.
Established Validation Department for Abbott pharmaceutical operatio...
1990 — 2000
Packaging Manager
Illinois
Responsible for the Packaging Operation, with more than 80 products in over 150 bottle and blister presentations, with app. 100 employees.
1988 — 1990
Manufacturing Manager
Illinois
Managed the 2nd shift of Manufacturing and Packaging operations.
1987 — 1988
Occupations
Executive
Chief Executive Officer
Director
Master of Science
Corporate Executive
Chief Executive
Operations Manager
Skills
Gmp
Validation
Pharmaceutical Industry
Technology Transfer
Fda
Capa
Cleaning Validation
21 Cfr Part 11
Project Management
Process Validation
Cross Functional Team Leadership
Pharmaceutical Process Technology
Quality By Design
Computer System Validation
Operations Management
Risk Management
Technical Transfers
Change Control
U.s. Food and Drug Administration
Pharmaceutical Process Development
Third Party Resource Management
Sop Development
Sop
Process Investigations
Equipment Qualification
Quality System
Dea
Ehs
Low and High Shear Granulation
Fluid Bed Granulation and Drying
Spray Drying
Wurster Particle Coating
Roller Compaction
Capsule Filling
Tableting
Tablet Coating
Bottle Filling
Blister Filling