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Fabiola Rivas Location
Lexington, KY, US
Fabiola Rivas Work
Validation Specialist @ (March 2025 - Present)
Quality Assurance and Validation Engineer @ (January 2022 - January 2024)
Operation Support and Project Manager @ (January 2020 - January 2022)
Document Control Specialist @ (January 2018 - January 2020)
Validation Project Manager @ (January 2014 - January 2018)
Material Management Associate @ (January 2012 - January 2014)
Fabiola Rivas Education
University of Kentucky
(English as a Second or Foreign Language/ESL Language)
2011-2012
Universidad Rafael Belloso Chacín
Bachelor's degree (Business Administration and Management, General)
1992-1996
Universidad Rafael Belloso Chacín 1992-1994
Fabiola Rivas Skills
Written Communication
High Quality Standards
Data Analysis
Teamwork
Interpersonal Skills
Document Review
Mathematics
Purchase Orders
Due Diligence
Data Management
Skilled Multi-tasker
Continuous Improvement
Communication
Document Management
Change Management
Manufacturing Operations
Attention to Detail
Pharmaceutical Industry
SOP
Quality Assurance
Quality System
Validation
GMP
Biotechnology
Quality Control
CAPA
21 CFR Part 11
Change Control
Technology Transfer
Inventory Control
U.S. Food and Drug Administration (FDA)
Manufacturing
Microsoft Office
Microsoft Excel
Microsoft Word
PowerPoint
QuickBooks
Outlook
Test Equipment
English
Aseptic Processing
New Product Validation
Hotmail
Physical Inventory
Bigfoot Sofware
Project Management
Production Equipment
Good Manufacturing Practice (GMP)
Collaboration Tools
Microsoft Teams
Virtual Collaboration
High Performer
Personal Development
Operations Management
Six Sigma
Email Management
Microsoft Outlook
Career Management
Leadership
Emotional Intelligence
Employee Coaching
Performance Management
Team Leadership
Building Trust
Goal Setting
Time Management
Standard Operating Procedure (SOP)
FDA
Social Media
Public Speaking
Microsoft PowerPoint
Wm Sap System Administrator
Corrective and Preventive Action Capa
Marketing
Customer Service
u.s. Food and Drug Administration Fda
FDA GMP
Controlled Material for Gmp Procedures
Research
Standard Operating Procedure Sop
Pharmaceutical Sales
Procedures
SOP development
Standard Operating Procedure
Corrective and Preventive Action
u.s. Food and Drug Administration
Fabiola Rivas Summary
Fabiola Rivas, based in Lexington, KY, US, is currently a Validation Specialist at Piramal Pharma Solutions. Fabiola Rivas brings experience from previous roles at Ortec Inc., PL Developments and Piramal Pharma Solutions. Fabiola Rivas holds a 2011 - 2012 University of Kentucky. With a robust skill set that includes Written Communication, High Quality Standards, Data Analysis, Teamwork, Interpersonal Skills and more. Fabiola Rivas has 1 emails and 2 mobile phone numbers on RocketReach.
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