Validation Engineer

What you’d do

Lead validation activities for facility equipment, utilities, processes, instrumentation, and computerized systems in a regulated environment. Author protocols and reports, coordinate qualification activities, and guide cross-functional teams and vendors. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• 5+ years in validation, engineering, or operations
• 4+ years in cGMP pharma, biotech, or medical device manufacturing
• SME in one or more validation disciplines