Ellab
Validation Engineering Specialist
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
Carlow, Ireland
Work mode:
Onsite
Published on:
28 August 2026
What they need
Exciting opportunity for you to join Carlow’s high‑performing manufacturing site to deliver safe, reliable medicines at global scale. We’re hiring a Validation Engineer to lead compliant, data‑driven qualification and validation across critical systems.
What you will do:
- Planning, scheduling and oversight of Periodic Revalidation & Initial Qualification studies.
- Responsible for setting and delivery of validation strategies.
- Lead and supports complex & critical investigations associated with validation and commercial activities.
- Co-ordinate multiple complex projects in parallel including but not limited New Product Introductions, Process Improvements and Investigations.
- Execution of Periodic Revalidation, Cycle Development & Initial Qualification studies as required.
- Technical review and approval of Periodic Revalidation, Cycle Development & Initial Qualification protocols & reports.
- Authoring and reviewing standard operating procedures and technical reports.
- Engage in the early stages of projects.
- Act as validation SME on the equipment within the area assigned
What skills you will need:
In order to excel in this role, you will more than likely have:
- Relevant technical qualification(s) in Applied Pharmaceutical / Biological / Computer / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.
- A minimum of 2-3 years directly related experience in pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
- SME in Cleaning Validation for reusable parts and process vessel washing and using Automated COP and CIP systems
- Knowledge of process monitoring systems, automation systems (DeltaV), operational intelligence & data systems (Pi System) within a GMP manufacturing environment would be beneficial and desirable.
If you are interested in hearing more please contact Cara Keegan on [email protected] or send your CV into [email protected].
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