Commissioning And Cleaning Validation

Descripción del Empleo:
Develop and execute commissioning, facility qualification and cleaning validations protocols and develop summary reports. Interface with customers on technical issues, project timeline, and commissioning/qualification/validation support. Actively participate on cross functional teams. Available to work in Puerto Rico or USA mainland.
Requisitos:
Engineering or Life Sciences bachelor degree. CQV, cleaning validation or relevant experience in the life pharmaceutical, medical devices or biotech 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.