Gregg Gazvoda
Technology and Quality Leader
- Role
- Vice President Information Systems, IT at Southern Research
- Location
- Madison, WI, US
- LinkedIn followers
- 500 followers
About Gregg Gazvoda
Regulatory Compliance | Validation Strategist | QA & IT Leadership As an accomplished Quality Assurance and IT Leader with extensive experience in the Biotech and Pharma industries, my background in Biotechnology, Quality, and IT has left me uniquely positioned to tackle the complex global regulatory landscape related to drug development (GLP, GCP, cGMP, and SOX). Areas of Expertise: Drug development, quality assurance, computer system validation, analytical instrumentation, equipment qualification, supplier/vendor assessment and management, project management, process optimization, business acquisition, integration, and expansion.
Experience
Vice President Information Systems, IT
Jan 2026 — Present · Birmingham, AL, US
Education
University of Wisconsin-Madison
Masters
University of Iowa
BS
Skills
- V&V
- Pharmaceutical Industry
- Sop
- Fda
- Validation
- Gmp
- Regulatory Requirements
- CRO
- Glp
- Computer System Validation
- Change Control
- Gcp
- Biopharmaceuticals
- U.s. Food and Drug Administration (Fda)
- Biotechnology
- Project Management
- Gxp
- Lims
- 21 Cfr Part 11
- Gamp
- Good Laboratory Practice (Glp)
- Capa
- Regulatory Affairs
- Toxicology
- Software Documentation
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