Vacancy caducado!
Description Details• Develop and manage GxP system lifecycle documentation, including Validation Plans, Testing Protocols, Traceability Matrix, Validation Reports• Work closely and communicate with project teams to analyze requirements and build test protocols• Author and execute test protocols to support computer system validation using HP Quality Center• Document bugs/defects using HP Quality Center• Follow FDA 21 CFR Part 11 regulations, GxP regulations, AbbVie policies/ procedures, GAMP5 best practices
• Proficient in the use of HP Quality Center• Communicate issues that could impact scope or timeline to validation team leadership• Complete all assigned training prior to due dates• Is detail oriented• Works under general supervision; typically reports to a manager• Enter project task time in Clarity• Requires a bachelor's degree and 4-7 years of experienceVacancy caducado!