We found the following information about Edward Brehm at Quidel, where Edward has worked as a Regulatory Affairs, Senior Manager since 2015. Edward's total work experience is over 35 years, during which time they had at least 19 jobs at different companies to develop skills. Edward studied at the Colorado State University from 1991. Edward Brehm currently lives in San Diego, California. You can contact with Edward by looking for phone or email address or get further information by requesting access to this professional's further details from SoftwareOfficial.
Name variants:
Ed Brehm,
Eddie Brehm,
Eddy Brehm,
Ned Brehm,
Ted Brehm,
Teddy Brehm,
Neil Brehm,
Tad Brehm
Last updated May 09, 2024
Contact Information
Workplace
Colleagues
Work History
Regulatory Affairs, Senior Manager
9975 Summers Ridge Rd, San Diego, CA 92121
Jun 1, 2015 — Apr 2019
Regulatory Affairs Manager
180 Hartwell Rd, Bedford, MA 01730
Apr 2014 — Jun 2015
Regulatory Affairs Manager
100 Abbott Park Rd, North Chicago, IL 60064
Regulatory Affairs Manager for the Alere Cholestech LDX product line at Alere (formerly Biosite)
Oct 2009 — Sep 2013
Regulatory Affairs Manager
Regulatory Affairs Manager for the Alere Cholestech LDX product line at Alere (formerly Biosite)
from Oct 2009
Regulatory Affairs Manager, Cmc
10390 Pacific Center Ct, San Diego, CA 92121
Aug 2003 — Nov 2008
Manager, Process Support, Operations Technical Support
San Diego, CA
Apr 2001 — Feb 2002
Associate Project Manager / Validation Engineer
San Diego, CA
Jul 2000 — Apr 2001
Senior Chemist
Fullerton, CA
Dec 1992 — Mar 1999
Education
1990 — 1991
1985 — 1990
1983 — 1985
1979 — 1983
Occupations
Executive
Manager
Scientist
Biotechnology Professional
Operations Manager
Biologist
Biological Scientist
Skills
Regulatory Affairs
IVD
FDA
CAPA
Biotechnology
Regulatory Submissions
GMP
ISO 13485
Medical Devices
Pharmaceutical Industry
Validation
Lifesciences
GLP
Sop
Clinical Trials
Clinical Development
IND
V&V
Vaccines
Quality System
Fda
Gmp
R&D
V&V
U.s. Food and Drug Administration
Capa
Life Sciences
Biologics
Iso 13485
Change Control
Glp
Ind
Biopharmaceuticals
Technology Transfer
Quality Assurance
Chemistry
Assay Development
Corrective and Preventive Action
Good Laboratory Practice
Research and Development
Standard Operating Procedure
Verification and Validation
Ivd
21 Cfr Part 11
IVD
GMP
Microsoft Office Suite
International IVD product registration