Validation Engineer

What you’d do

Lead validation activities for facility equipment, utilities, processes, instrumentation, and computerized systems, authoring protocols and reports and guiding cross-functional teams. Full time, coordinating qualification work with internal stakeholders and external vendors. 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 in a regulated environment
• 4+ years in cGMP pharma, biotech, or medical device manufacturing
• SME expertise in one or more validation disciplines
• Protocol and report authoring