About this role
Sr. Validation Project Lead - Medical Device at Compli, LLC (affiliate of George Butler Associates). Location: Richmond or Baltimore. Role: Support commissioning, Prepare reports, Coordinate execution Requirements: 7+ years CQV experience with aseptic utilities; BS in life sciences; strong technical writing; able to manage multiple projects; willing to travel locally. Category: Engineering Seniority: Senior Level Tools: Microsoft Word, Microsoft Excel, PowerPoint, Microsoft Project, Documentation tools Commitment: Full Time Workplace: Onsite Languages: English