Tenovi is hiring a Quality & Regulatory Specialist to manage the day-to-day quality system operations and keep FDA listings and device labeling compliant. This full-time individual contributor role collaborates with our regulatory advisor to roll out procedures, train staff, and maintain records in accordance with QMSR and ISO 13485.
You will perform receiving inspection, handle nonconformances and CAPAs, manage document control, and support internal and FDA audits.
#J-18808-LjbffrQuality & Regulatory Systems Specialist in irvine at Unknown Company
This position is listed as full time and onsite.