Verista, located in Indianapolis, IN, seeks a qualified professional to lead VHP cycle development for pharmaceutical isolators and ensure adherence to regulatory GMP standards. You will design validation strategies, author PQ protocols, and collaborate with Validation, Engineering, Manufacturing, and Quality teams to drive compliant lifecycle management.
Required are hands-on VHP experience, aseptic processing knowledge, BI placement skills, and strong technical writing abilities.
#J-18808-LjbffrProject Engineer – VHP Decontamination & Isolator Systems in indianapolis at Unknown Company
This position is listed as full time and onsite.