Craig Graver

Vice President, Global Quality Systems and Compliance

Craig Graver is a skilled professional, that works in Amri (Albany Molecular Research Inc.) main office of which is in 998. as a Vice President, Global Quality Systems and Compliance from 2020. Craig has earned professional experience in more than eight positions at various companies. Craig Graver went to the Temple University and was studying there from 2006 to 2010. Huntsville, Alabama is the city, where the professional was lastly known to be settled. The professional's e-mail and phone can be easily accessed through SoftwareOfficial on demand.
Name variants:
Craig Graver
Last updated Jul 06, 2024

Contact Information

Last Update
Jul 1, 2022
Email
cg**@amriglobal.com, cg**@luitpold.com, cw**@comcast.net
Location
Huntsville, AL

Workplace

AMRI (Albany Molecular Research Inc.)
Vice President, Global Quality Systems and Compliance

Albany, NY

Industry

Pharmaceuticals

Work History

Vice President, Global Quality Systems and Compliance

26 Corporate Cir, Albany, NY 12203
from 2020

Director- Quality Control and Gmp Compliance

Shirley, NY
2012 — 2015

Senior Director, Quality Control

3250 Commerce Pkwy, Miramar, FL 33025
2008 — 2012

Associate Director, Pharmaceutical Analysis

1998 — 2008

Manager, Quality Control

Pennsylvania
1992 — 1998

Research Scientist Iii

1989 — 1992

Laboratory Supervisor

2320 Scientific Park Dr, Wilmington, NC 28405
1987 — 1989

Chemical Technician

1984 — 1987

Education

Occupations

Executive
Vice President
Chief Executive

Skills

Gmp
Capa
21 Cfr Part 11
Quality System
Fda
Pharmaceutical Industry
Change Control
Validation
Cleaning Validation
Sop
Glp
Quality Auditing
Aseptic Processing
Quality Assurance
Biopharmaceuticals
Lims
Technology Transfer
Usp
Analytical Chemistry
Hplc
Private Investigations
V&V
Gxp
Biotechnology
Chromatography
Pharmaceutics
Drug Delivery
Compliance Remediation
Regulatory Affairs
Regulatory Submissions
Trackwise
Computer System Validation
Corrective and Preventive Action
Formulation
Cmc Regulatory Affairs
U.s. Food and Drug Administration
Good Laboratory Practice
Standard Operating Procedure
Good Manufacturing Practice
Cgmp Quality Systems
Investigations and Capa
Developing and Validating Analytical Methodology
Fda Gmp
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