The Role
Performs pharmaceutical quality assurance and validation activities, including facilities and utilities commissioning, computer system validation, equipment validation, risk assessments, change controls, SOP management, data integrity, documentation review, and syringe/vial inspection processes. Uses KNEAT, CDOCS, SCADA, TrackWise, and MAXIMO systems while applying risk management and decision-making techniques.
Summary Generated by Built In
- Facilities and Utilities Commissioning and Qualification,
- Computer System Validation,
- Equipment validation,
- Risk Assessments,
- KNEAT,CDOCS, SCADA, TRACKWISE,MAXIMO
- Good Documentation Practices, Data Integrity
- Change Controls,
- Standard Operation Procedure
- Syringe/Vials Inspection Process
- Documents revision and approval
- Strong knowledge in Decision Making Techniques
- Risk Management
Requirements
-Doctorate + 2 years of directly related experience OR
-Masters + 4 years of directly related experience OR
-Bachelors + 6 years of directly related experience OR
-Associates + 10 years of directly related experience OR
-High school/GED + 12 years of directly related experience
Skills Required
- Doctorate degree and 2 years of directly related experience
- Master's degree and 4 years of directly related experience
- Bachelor's degree and 6 years of directly related experience
- Associate's degree and 10 years of directly related experience
- High school diploma or GED and 12 years of directly related experience
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The Company
What We Do
ISPV Inc. is a Life Science company that leads Productivity & Validation projects for the Pharmaceutical and Food industries.
