Engineer - Process Development (Commissioning, Qualification, and Validation)

What you’d do

Support commissioning, qualification, and validation of GMP equipment and processes for Final Drug Product operations. Author and implement IQ/OQ/PQ protocols and validation plans, and maintain validated state through periodic review. Full time. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• Engineering and scientific principles for GMP systems
• Author and implement IQ/OQ/PQ protocols
• Validation lifecycle documentation
• Equipment and system design review
• Knowledge of regulatory requirements