Rich Levy
Editor , Pda Journal of Pharmaceutical Science and Technology
Since 2005, Rich Levy has been working in Parenteral Drug Association (PDA). Rich Levy is a qualified Senior Vice President with over 18 years of work experience. According to Rich's resume and work profile, this person has worked at more than three companies with diverse backgrounds and gained various skills. Rich attended school at the Worcester Polytechnic Institute, Worcester, MA from 1981 to 1985. Rich can be found in Washington, DC – where this expert is currently located. You can search for Rich Levy's contacts. We can also provide you with detailed contact information upon request.
Name variants:
Richard Levy
Last updated Jun 15, 2024
Contact Information
Last Update
Jul 12, 2022
Email
le**@pda.org
Location
Washington, DC
Workplace
Colleagues
Work History
Senior Vice President
Dr. Levy is currently Senior Vice President of Scientific and Regulatory Affairs at the Parenteral Drug Association (PDA) in Bethesda Maryland. In this capacity, he is responsible for direc...
from 2005
Corporate Vice President
Dr. Levy was Corporate Vice President and General Manager of PAREXEL Consulting, a newly formed PAREXEL International business unit created by the merger of KMI, Barnett, and Worldwide Regul...
2002 — 2005
Director
Dr. Levy was with Millipore Corporation for 16 years in a variety of Business, R&D, Regulatory and Quality Systems positions. He was responsible for elements of the microbiological and ...
Jan 1986 — Dec 2001
Education
1981 — 1985
1972 — 1975
1968 — 1972
Occupations
Writer
Editor
Executive
Senior Vice President
Vice President
Chief Executive Officer
Chief Executive
Corporate Executive
Skills
Validation
Regulatory Affairs
Pharmaceutical Industry
Gmp
Aseptic Processing
Microbiology
Biotechnology
Fda
Biopharmaceuticals
Technology Transfer
Quality System
Pharmaceutics
R&D
Sterilization
Chromatography
Change Control
Capa
V&V
Regulatory Submissions
Regulatory Requirements
Glp
21 Cfr Part 11
Management
Clinical Development
Drug Development
Vaccines
Quality Assurance
Lifesciences
Medical Devices
Manufacturing
Sop
Strategic Planning
Clinical Trials
Gxp
Quality Auditing
Publications
Pharmaceutical Microbiology
Filtration
Drug Discovery
Commercialization
Formulation
Gcp
Cro
Drug Delivery
Iso 13485
Analytical Chemistry
Cleaning Validation
Ind
Biologics
Computer System Validation