About this role
Validation Engineer at Syner-G. Location: Boston, Massachusetts, United States. Role: executing validation, writing protocols, performing walkdowns Requirements: Bachelor's in life science, 3+ years biotech/pharma/medical device validation experience, knowledge of FDA cGMP, FMEA, CSV, protocol generation and IQ/OQ/PQ reporting, strong written/verbal communication. Category: Research and Development (R&D) Seniority: Mid Level Tools: FDA cGMP, FMEA, Computerized System Validation (CSV), Piping and Instrumentation Diagram (P&ID) Commitment: Full Time Workplace: Onsite Languages: English