Description
A world leading pharmaceutical manufacturing plant has a long-term contract requirement for an experiencedValidation Engineer to work on a sterile project, within a newly built manufacturing facility. This new building will house two products and we are seeking individuals with a mixed background and skill set to complete and number of activities.The focus of this role is the Performance Qualification and Process Validation, therefore, you will need to have an excessive working knowledge on the following:
- Cleaning validation (Clean in place systems)
- Facility qualification
- Clean Utilities (WFI, Pure Steam, Clean Comp Air)
- Terminal sterilisation by autoclave
Requirements
- Engineering / Validation / Process background
- Knowledge / understand equipment and services
- Can produce documentation to GMP and regulatory standard – IQs, OQs, PQs etc
- At least 2 years’ experience in pharma
- Good communication skills “Verbal & written” (customer focused)
- Able to cope with fast moving, compliant, quality driven focus & tasks
If this long term opportunity, paying competitive rates, working with cutting edge technology is of interest, then please contact me immediately.