Job 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.
Apply for this Position
Ready to join QRC Group, LLC? Click the button below to submit your application.
Submit Application