Peter Stiffel Email & Phone Number
Senior Director, Quality Compliance, Corporate Quality Professional Services @ Teva Pharmaceuticals
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Peter Stiffel Location
- Pomona, NY, US
Peter Stiffel Work
- 2010 -now Senior Director, Quality Compliance, Corporate Quality Professional Services @
- 2007 -2010 Global Director, Quality Systems @ Barr Pharmaceuticals Teva Pharmaceutical
- 2004 -2007 Director Quality Assurance @
- 1996 -2006 Associate Director, QA; Regulatory Compliance @
- 1989 -1996 Plant Manager @
- 1985 -1988 Manufacturing Manager @ Chelsea Laboratories
- 1982 -1985 Packaging Manager @ Chelsea Laboratories
- 1978 -1982 Packaging Supervisor @
Peter Stiffel Skills
- Investigations
- Quality Management
- Clinical Trials
- Computer System Validation
- HPLC
- Private Investigations
- GMP
- ISO 13485
- GxP
- Regulatory Affairs
- Life Sciences
- Validation
- Process Improvement
- Trackwise
- Quality Assurance
- Cleaning Validation
- Regulatory Requirements
- Quality by Design
- Quality System
- Analytical Chemistry
- Lifesciences
- V&V
- Quality Auditing
- Pharmaceutics
- USP
- Manufacturing
- Drug Development
- GCP
- Regulatory Submissions
- ANDA
- Quality Control
- Pharmaceutical Industry
- Technology Transfer
- GLP
- LIMS
- CAPA
- FDA
- Sop
- 21 CFR Part 11
- Biopharmaceuticals
Peter Stiffel Summary
- Peter Stiffel, based in Pomona, NY, US, is currently a Senior Director, Quality Compliance, Corporate Quality Professional Services at Teva Pharmaceuticals. Peter Stiffel brings experience from previous roles at Barr Pharmaceuticals Teva Pharmaceutical, Barr Pharmaceuticals and Barr Laboratories. With a robust skill set that includes Investigations, Quality Management, Clinical Trials, Computer System Validation, HPLC and more. Peter Stiffel has 1 emails on RocketReach.
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