Resultados de la búsqueda: 2 vacantes
...in Puerto Rico & USA
Responsibilities:
Developing and managing GMP system lifecycle documentation, including Validation Plans, User Requirements Specifications, Functional and Design Specifications, Testing Protocols (IQ/OQ/PQ), User Acceptance testing,...
...and documentation necessary to assure compliance according to the appropriate federal and international regulations which govern the user's applications.
Reports on the status of validation activities to fulfill regulatory requirements. Keeps abreast of changing...
