Addresses and responds to all product inquiries, complaints, and suspected adverse events in a timely and appropriate manner and in compliance with US regulations (FDA, USDA, EPA), relevant GMPs, BIVI policies and procedures for the capture, maintenance and reporting of adverse events and product quality complaints. Some of the Your Responsibilities Receive all product in

Perform Smoke studies and assist in semi annual Media fill qualifications as a SME Perform requalification/periodic review of autoclaves, depyrogenation tunnels, cold rooms, freezers and warehouse areas. Has worked with Ellabs data loggers and software Write and execute protocols and complete final reports. Understanding of cleaning validation concepts and principles. Und

Perform Smoke studies and assist in semi annual Media fill qualifications as a SME Perform requalification/periodic review of autoclaves, depyrogenation tunnels, cold rooms, freezers and warehouse areas. Has worked with Ellabs data loggers and software Write and execute protocols and complete final reports. Understanding of cleaning validation concepts and principles. Und

REMOTE Part Time (20 hrs per week0 Business Hours Responsibilities This is a chief coordinator role The position focuses on logistics for managing product case series conducted at KEE/customer clinics Skills or Requirements Ability to communicate effectively with medical professionals Understanding of terminology Ability to take direction and communicate with core stakeho