- Houston, Texas, United States
- 5+ years
Support Computer System Validation activities for pharmaceutical manufacturing automation systems.
Responsibilities
- Develop and maintain validation documentation
- Prepare and review requirements, functional specifications, risk assessments, and traceability matrices
- Develop and execute validation test protocols
- Review automation system documentation for alignment with validation requirements
- Support validation of Emerson DeltaV, Rockwell PLC, and vendor package equipment
Requirements
- Nice to have: Kneat Power User
- Nice to have: Veeva Vault
- Nice to have: FactoryTalk AssetCentre
- Nice to have: AVEVA PI
- Nice to have: industrial automation applications