Manufacturing Eng. I (Pv/ Software Validation)

Descripción del Empleo:
Overall Process validation. Works under general supervision. Follows established procedures. Work is reviewed for soundness of technical judgment and overall adequacy.
Contributes to the completion of milestones associated with specific projects. Failure to achieve results or erroneous decisions or recommendations may cause delays in program schedules and may result in the allocation of additional resources.
Develops/implements production/processing methods and controls to meet quality standards in most cost efficient manner. Investigates and resolves work-in-process problems. Recommends and implements improvements and/or modifications in sequence of operations, equipment utilization and related matters. Monitors assigned operations to assure compliance with approved methods and standards. Typically would possess a degree in Engineering.
Requisitos:
3 to 5 years of experience
Fluency speaking and writing in English and Spanish.
Experience in medical device, pharmaceutical, or electronic industry.
Root Cause Analysis
Validation experience (process validation/ software validation/ process characterizations)