Validation Engineer – Ireland – Pharmaceuticals – Contract
Do you want to be involved with exciting pharmaceutical projects?
When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Validation Engineer.
This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.
Essential Duties and Responsibilities for this role include, but are not limited to, the following:
1. Design/Author/Review/Approve/Execute qualification/validation documentation and cycle development studies in line with the standard approval process.
2. Design/Author/Review/Approve/Execute Execution/development of change controls.
3. Resolving technical issues encountered during study execution.
4. Engagement with Production, Maintenance and Quality representatives in the assigned area of operations during execution of Cycle Development & Performance Qualification activities.
5. Technical input into quality notification by authoring/reviewing/approving investigations.
6. Perform root cause analysis of system failures, substandard performance, using standard tools and methods, to resolve machine and system issues.
7. Support continuous improvement through Lean Six Sigma methodologies.
8. Serve as validation representative for cross functional projects and represent the validation team at global technical forums.
Desirable Experience:
1. Experience in cleaning validation including but not limited to CD & PQ of mobile vessels (CIP) and parts washers (COP).
2. Relevant technical qualification(s) in Applied Pharmaceutical / Biological / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.
3. Exception / Deviation Management and Change Control.
4. Demonstratable experience of leading technical related projects.
5. Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable.
6. Evidence of continuous professional development is desirable.
If this role is of interest to you, please apply now
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