Dwain Allen

Director Regulatory Affairs

Dwain Allen is a highly qualified professional, who works in Avanir Pharmaceuticals main office of which is in 615. on the position of Associate Director, Regulatory Affairs from 2012. Dwain Allen has earned professional experience in more than 12 positions at various companies. Dwain Allen went to the University of Arizona and was studying there from 1981 to 1984. San Marcos, California is the area, where this professional was known to live. Their email address and phone number can be accessed through this website on demand.
Name variants:
Dwain Allen
Last updated May 08, 2024

Contact Information

Last Update
Jul 7, 2022
Email
dw**@pacira.com
Location
San Marcos, CA

Workplace

Avanir Pharmaceuticals
Associate Director, Regulatory Affairs

Aliso Viejo, CA

Industry

Pharmaceuticals, Pharmaceutical Preparations, Pharmaceutical Preparations & Research, Pharmaceutical Preparation Manufacturing, Pharmaceutical Preparation Mfg

Work History

Associate Director, Regulatory Affairs

Aliso Viejo, CA
from Apr 2012

Director, Regulatory Affairs

San Diego, CA
Oct 2008 — Apr 2012

Sr. Manager, Regulatory Affairs

Aliso Viejo, CA
Jun 2005 — Sep 2008

Manager, Regulatory Affairs

San Diego, CA
Feb 2004 — Jun 2005

Q.A. Compliance Manager

Irvine, CA
2002 — 2004

Professional Services Manager

Irvine, CA
1999 — 2002

Senior Specialist, Regulatory Affairs

Irvine, CA
1996 — 1999

Manager, Regulatory Affairs

South El Monte, CA
1995 — 1996

Senior Specialist, Regulatory Affairs

South El Monte, CA
1991 — 1995

Manager, Clinical Research

San Dimas, CA
1990 — 1991

Clinical Research Associate

Los Angeles, CA
1987 — 1990

Senior Laboratory Technician

Los Angeles, CA
1986 — 1987

Education

Occupations

Executive
Director
Deputy Director
Operations Manager
Deputy Manager
Chief Executive

Skills

Laboratory
Clinical Trials
Medical Writing
Cro
Hplc
Gmp
Ectd
Clinical Research
Regulatory
Biotechnology
Regulatory Affairs
Change Control
Validation
Medical Devices
Regulatory Requirements
Pharmacovigilance
Drug Discovery
Lifesciences
V&V
Oncology
Drug Development
Gcp
Clinical Development
Pharmaceutics
Regulatory Submissions
Formulation
Pharmaceutical Industry
Technology Transfer
Aseptic Processing
Glp
Therapeutic Areas
Capa
Fda
Sop
21 Cfr Part 11
Ind
Biopharmaceuticals
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