Cqv Specialist

Descripción del Empleo:
Develop and execute equipment and process validations (CSV, IQ, OQ, PQ) on manufacturing and packaging equipment, develop summary reports. Interface with customers on technical issues, project timeline, and validation support. Actively participate on cross functional teams. Available to work in Puerto Rico or USA mainland.
Requisitos:
CQV or relevant experience in the life science regulated industry. Engineering or science degree from a recognized institution. Ability to effectively communicate verbally and in writing. Must be able to plan, coordinate, perform, and supervise contract staff with minimal oversight. Ability to apply working knowledge of applicable regulatory standards (FDA, ISO, OSHA, EPA, CFR, etc.) and good understanding in GMP requirements and validation processes.