Description
Validation Engineer role for a contracted medical devices position in Añasco, Puerto Rico, focused on validation services within the Quality/Validation area. The job involves developing and executing IQ/OQ/PQ protocols and reports, supporting validation for manufacturing processes, equipment, cleaning, and computerized systems, performing change control impact assessments, analyzing data with statistical tools, and maintaining compliance with GDP, FDA, ISO, and cGMP requirements. Requires an engineering bachelor's degree, at least two years of validation experience in pharmaceutical or medical devices, and fluency in Spanish and English.
