DemoExample roles for this demo. These jobs are not real.
Equipment and computer system validation for a new sterile filling line, from protocol writing through to final report.
What you’ll do
- Write and run IQ, OQ and PQ protocols
- Support computer system validation to GAMP 5
- Handle deviations and change controls
- Work alongside engineering and QA to hit the line start-up date
What you’ll need
- Previous validation contracts in a GMP environment
- Sterile or aseptic manufacturing experience
- Available to start within four weeks
About the employer
Pharmaceutical manufacturer in Oxfordshire. We share the employer’s name when we speak to you about the role. Questions first? Call us on 07884 493960 and quote NLS-1037.