Robert Sciascia's Location
Easton, Pennsylvania, United States
Robert Sciascia's Work
- QA Validation Specialist @ Novartis Oncology
- Sanofi Genzyme Ridgefield NJ, Senior Validation Specialist at CTG @ Sanofi
- Merck in Lansdale Pa, Project CQV Lead at Precis Commissioning @ Merck
- Roche, Branchburg NJ, CQV Specialist at Avex Consulting @ Roche
- Novartis Morris Plains NJ, CQV Specialist at Compliance Technology Group (CTG) @ Novartis
- Sanofi Ridgefield NJ, CQV Specialist at Compliance Technology Group (CTG) @ Sanofi
- CQV Specialist at Yoh for J and J Janssen @ 1205
- Sanofi Pasteur, CQV Specialist at Compliance Technology Group (CTG) @ Sanofi
- Commissioning and Validation (CQV) Specialist at Intuitive Technology Group @ McNeil Consumer Healthcare
- Commissioning and Validation (CQV) Specialist at IPS @ IPS-Integrated Project Services
Robert Sciascia's Education
- Lincoln Technical Institute
Associate Degree Earned (Electronic Technology)
1983 - 1985 - Northampton County Community College
Robert Sciascia's Skills
- Quality Management
- Laboratory
- Validation Master Plans
- Cross Functional Team
- Equipment Qualification
- Computer System Validation
- Root Cause Analysis
- GAMP
- GMP
- GxP
Robert Sciascia's Summary
Robert Sciascia, based in Easton, Pennsylvania, United States, is currently a QA Validation Specialist at Novartis Oncology, bringing experience from previous roles at Sanofi Genzyme, Merck, Roche and Novartis. Robert Sciascia holds a 1983 - 1985 Associate Degree Earned in Electronic Technology @ Lincoln Technical Institute. With a robust skill set that includes Quality Management, Laboratory, Validation Master Plans, Cross Functional Team, Equipment Qualification and more, Robert Sciascia contributes valuable insights to the industry. Robert Sciascia has 2 emails on RocketReach.
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