Found Description
Job Description
Process Validation Specialist with experience in ethylene oxide (ETO) sterilization processes comply with applicable regulatory, quality, and industry standards, guaranteeing process effectiveness, reproducibility, and safety for medical or industrial products.
Responsibilities:
- Develop, execute, and document IQ/OQ/PQ validation protocols for ETO sterilization processes.
Ready to Apply?
Submit your application for Process Validation Specialist (ETO) at QRC Group, LLC
Apply Now