Exciting Pharmaceutical Projects
We invite you to join our client, a Centre of Excellence in veterinary vaccine development and production.
This is a leading pharmaceutical company with the largest centre in the industry worldwide, employing over 1000 people. They require a Validation Engineer to add to their team.
About the Role
This is a fantastic opportunity to be involved with critical investment projects both on-site and remotely.
* Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process.
* Design/Author/Review/Approve/Execute Execution/development of change controls.
* Resolving technical issues encountered during study execution.
* Engagement with Production, Maintenance and Quality representatives in the assigned area of operations during execution of Cycle Development & Performance Qualification activities.
* Technical input into quality notification by authoring/reviewing/approving investigations.
* Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues.
* Serve as validation representative for cross functional projects and represent the validation team at global technical forums.
Desirable Experience
The successful candidate will have:
* Experience in cleaning validation including but not limited to CD & PQ of mobile vessels (CIP) and parts washers (COP).
* Relevant technical qualification(s) in Applied Pharmaceutical / Biological / Chemical sciences or applied Technical / Engineering qualification.
* Exception / Deviation Management and Change Control.
* Demonstratable experience of leading technical related projects.
* Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment.
* Evidence of continuous professional development.