DescripciónDescription
QA/Validation Specialist to review validations documents, and/or reviewing/auditing documentation from quality view point; knowing the requirements of each of the stages.
Must have knowledge with:
Quality Validation Documentation
Protocols Design
IQ/OQ/PQ Execution
Technical Documentation
Validation Activities
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Requisitos Requirements
Bachelor of Sciences/Engineering
Five (5) years of experience in the Medical Devices industry
?Bilingual (Spanish/English)
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Empleos en Puerto RicoJobs in Puerto Rico
QRC GROUP LLC
Empleos en Puerto RicoJobs in Puerto RicoProfesionales
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