About this role
CQV/Validation Engineer at Sebela Pharmaceuticals. Location: Holbrook, Massachusetts, United States. Role: supporting validation, developing documentation, executing qualification Requirements: Bachelor's in Engineering or Life Sciences, 3+ years FDA-regulated validation experience; knowledge of equipment/utility/process/cleaning/computerized system validation, cGMP, 21 CFR Part 11 preferred; strong technical writing; AutoCAD preferred. Category: Engineering Seniority: Mid Level Tools: AutoCAD Commitment: Full Time Workplace: Onsite Languages: English