Rich Baritot is a high-skilled expert, working in Coda Corp USA on the position of Director of Validation from 2002. Rich has earned professional experience in more than four positions at different companies. Rich Baritot went to the State University of New York Empire State College and got education from 1992 to 1996. This expert has such professional qualifications as Change Management Specialist (Cms), Six Sigma Lean Professional (Sslp), and Six Sigma Black Belt Professional (Ssbbp). Rochester, New York is the area, where this professional was known to be living. The professional's phone and email can be easily accessed through SoftwareOfficial on demand.
Name variants:
Richard Baritot
Last updated Jun 11, 2024
Contact Information
Last Update
Jun 30, 2022
Email
rb**@codacorpusa.com
Location
Rochester, NY
Company
Coda Corp USA
Workplace
Director of Validation
Work History
Director of Validation
Responsibilities include but are not limited to working with customers to develop validation project plans, write functional specifications, write test protocols and procedures, develop func...
from 2002
Validation Project Leader
Working with clients to develop and implement validation project plans, quality system auditing, developing system user requirements and functional specifications, writing and execution of t...
Aug 1997 — Mar 2008
Senior Validation Specialist
Responsibilities included but were not limited to the specification, installation, operation, maintenance, programming, calibration, and validation testing of a variety of information system...
1989 — 1997
Sonar Technician
Responsibilities included but were not limited to the operation, programming, calibration, preventative maintenance, troubleshooting and repair of shipboard SONAR, oceanographic, fire-contro...
1987 — 1989
Education
Occupations
Accountant
Account Manager
Executive
Director
Project Manager
Operations Manager
Project Managers
Skills
Validation
V&V
Fda
Medical Devices
Computer System Validation
Gmp
Capa
Quality System
Change Control
Testing
21 Cfr Part 11
Design Control
Quality Auditing
Gxp
Iso 13485
Technology Transfer
Quality Assurance
Quality Management
Root Cause Analysis
Sop
Quality Control
Troubleshooting
Glp
Aseptic Processing
Software Documentation
Research and Development
Pharmaceutical Industry
Gamp
Lims
Regulatory Affairs
Biotechnology
Process Simulation
Regulatory Submissions
Pharmaceutics
Cross Functional Team Leadership
Calibration
Manufacturing
Verification and Validation
R&D
Design of Experiments
Project Management
Lean Manufacturing
Six Sigma
Iso Standards
Continuous Improvement
Regulatory Requirements
Leadership
Business Strategy