A consulting firm in pharmaceutical services is seeking a Computer System Validation (CSV) Specialist for a 12-month on-site role in Edmonton. This position requires experience in IT Qualification and CSV in GMP-regulated environments, as well as strong documentation and communication skills. The CSV Specialist will develop and execute validation protocols, qualify laboratory equipment, and ensure compliance with regulatory standards. If you are a validation professional ready for your next opportunity, apply now. #J-18808-Ljbffr
Job Title
Onsite CSV Specialist for GMP Lab Validation (Edmonton)