Quality Systems Engineer

What you’d do

Under close supervision, supports the facility's Quality Plan by writing and implementing process validation and GMP procedures, drafting validation protocols and reports, and maintaining validation records and Risk Management Files. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• 0–2 years quality engineering or process validation experience
• Master's degree may substitute for prior work experience
• Knowledge of FDA and GMP requirements
• Validation protocol and report writing