A recent new opportunity has come along for multiple engineers to be brought on board in this exiting new phase of development in a pharmaceutical company.
We have a requirement for a Validation Engineer to join an independent automation systems integrator, dedicated to increasing the visibility of real-time information to improve the performance of manufacturing and processing companies.
- You will be required as a Validation Engineer for ensuring that all manufacturing processes, packing operations, equipment, cleaning, utilities/facilities, computer and analytical methods are fully validated to meet the expected and operational requirements and GMP regulatory requirements.
- Working knowledge in Validation (Computer System/Process/Project/Equipment/Cleaning etc.) within the Biotech/Med Device/ Pharmaceutical (FDA/MHRA regulated industries).
cGMP, GAMP and GxP knowledge with knowledge of FDA 21 CFR Part 11, Annex 11 regulation.