About this role
Sr. Validation Project Lead - Medical Device at Compli, LLC. Location: Richmond or Baltimore. Role: Support validation, Coordinate protocols, Prepare reports Requirements: 7+ years CQV experience with aseptic liquids, BS in life sciences; strong technical writing; able to manage multiple projects; proficient in GMP/QA practices. Category: Engineering Seniority: Senior Level Tools: Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project Commitment: Full Time Workplace: Onsite Languages: English