About this role
Validation Engineer at Cryoport. Location: Irvine, California, United States. Role: overseeing qualifications, developing reports, engaging clients Requirements: 2+ years in Biopharmaceuticals/medical devices; experience writing client-facing docs; ISO/IATA/ISTA knowledge; QC/validation skills; proficient with Excel and MS Office; project management a plus. Category: Engineering Seniority: Mid Level Tools: Excel, Pivot Tables, Microsoft Office, PowerPoint, Teams Commitment: Full Time Workplace: Onsite Languages: English