MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. * Collaborate with cross-functional teams including IT, Quality Assurance, and Operations to ensure documentation and validation of systems according to internal procedures * Maintain the inventory of software applications * Conduct periodic reviews and improve existing documentation of systems * Prior experience in Computerized System Validation within a regulated industry (e.g., pharmaceuticals, biotechnology, medical devices) or basic knowledge of regulatory requirements and guidelines, or certification (FDA 21 CFR Part 11, GxP, etc.) would be beneficial
mehr