Description:
Title: Validation Engineer Preferably from a Medical Device Background Location: Raynham, MA (Onsite) Duration: 12 Months+ Key Responsibilities: - Writing and execution of validation protocols and reports (i.e., IQ, OQ, PQ, etc.). - Developing and implementing manufacturing processes; preparation of specifications and operator instructions; process studies; production readiness; investigations; root cause analysis; problem solving; and report/presentation preparation. - Updating procedures, man
Jan 26, 2026;
from:
dice.com