Collaborate with cross-functional teams including IT, Quality Assurance, and Operations to ensure documentation and validation of systems according to internal procedures * Stay up to date with industry trends, regulatory changes, and best practices in computerized system validation * Any 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 - MED-EL Medical Electronics * Innsbruck * Befristeter Vertrag * Vollzeit - About MED-EL - 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 b
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