Offer summary
Qualifications:
BA/B.S. in relevant field preferred, 5+ years in FDA regulated domain, 3+ years in Computer System Validation, Knowledge of medical device and CSV standards, Ability to work under minimal supervision.
Key responsabilities:
- Lead verification, validation and maintenance activities
- Support regulatory compliance for Tempus Medical Devices
- Develop and maintain CSV policies and procedures
- Perform software validation and change controls
- Provide guidance and mentorship to test engineers