About this role
Sr. Validation Project Lead - Medical Device at Compli, LLC. Location: Richmond or Baltimore. Role: Support validation, Prepare documents, Coordinate protocols Requirements: 7+ years CQV experience with aseptic liquid fill utilities; life sciences degree; strong technical writing; MS Office; regulatory knowledge. Category: Engineering Seniority: Senior Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project Commitment: Full Time Workplace: Onsite Languages: English