Roger Halbert

Director of Analytical Services

Since 2019, Roger Halbert has been working in Oxford Pharmaceuticals situated 144, 144. This person is a well-qualified Director of Analytical Services with over 16 years of work experience. According to Roger's resume and work profile, Roger has worked at more than seven places with numerous backgrounds and got different skills. Roger attended school at the East Carolina University from 1993 to 1996. Roger Halbert can be found in Myrtle Beach, South Carolina – where this expert is currently located. You can search for the professional's email address and phone number. We can also provide you with additional contact information upon request.
Name variants:
Rodger Halbert, Rod Halbert, Roddy Halbert, Rodge Halbert, Roge Halbert
Last updated Jun 16, 2024

Contact Information

Last Update
Jul 10, 2022
Email
ch**@aol.com
Location
Myrtle Beach, SC

Workplace

Director of Analytical Services

Birmingham, AL

Industry

Mfg Pharmaceutical Preparations

Work History

Director of Analytical Services

301 Leaf Lake Pkwy, Birmingham, AL 35211
from Oct 2019

Associate Director of Quality Control

Dec 2017 — Oct 2019

R and D Manager Analytical Method Validations

318 Mccullough Ave, San Antonio, TX 78215
Sep 1, 2011 — Mar 1, 2012

Principal Consultant

Consulting on pharmaceutical cGMP. Specializing in laboratory remediation, management, SOP and systems development, investigations and CAPA. Expertise in analytical method development and va...
from Mar 1, 2012

Director of Analytical Sciences

Mar 2008 — May 2011

Accounts Receivable and D Manager

Nov 2000 — Mar 2008

Qc Chemist

Illinois
1996 — 1998

Occupations

Executive
Director
Director of Quality Control
Supporting Member
Operations Manager
Compliance Manager
Team Member

Skills

Validation
Gmp
Capa
R&D
Analytical Chemistry
Pharmaceutical Industry
Sop
Fda
Glp
Hplc
Quality Control
Chemistry
Pharmaceutics
Method Development
Gxp
V&V
Lims
Technology Transfer
21 Cfr Part 11
Laboratory
Research and Development
High Performance Liquid Chromatography
U.s. Food and Drug Administration
Regulatory Affairs
Change Control
Regulatory Requirements
Cleaning Validation
Ind
Quality Auditing
Gas Chromatography
Uv/Vis
Quality Assurance
Computer System Validation
Regulatory Submissions
Wet Chemistry
Drug Development
Cro
Clinical Trials
Standard Operating Procedure
Good Laboratory Practice
Corrective and Preventive Action
Trackwise
Contract Manufacturing
Usp
Analytical Method Validation
Fda Gmp
Science
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