Find a jobRecruiters

Validation Engineering Specialist

Exclusive opportunity

Onsite

Validation Engineering Specialist

Ellab

Validation Engineering Specialist

Skills

Process Improvement

2 months ago

Share this opportunity

Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.

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].

Other offers great for you!

These companies are also looking for great profiles

Visian

AI Data Engineering

Freelance

Paris, France

Hybrid

Top Recruiter

Skills

Data Engineering

5 days ago

Quick apply

Vorstone

Ingénieur Validation & Qualification Technique Embarquée (H/F)

500

Freelance

93160 Noisy-le-Grand, France

Onsite

Skills

IVVQValidation SystèmeQualification TechniqueTest EngineerValidation EmbarquéeIntégration & ValidationTest & Validation EngineerQualification ProduitTests FonctionnelsTests de Non-RégressionBancs de TestsElectroniqueSystèmes Embarqués.

5 days ago

Quick apply

Vorstone

Ingénieur Validation / Testeur

500

Freelance

93160 Noisy-le-Grand, France

Onsite

Skills

IVVQValidation SystèmeQualification TechniqueTest EngineerValidation EmbarquéeIntégration & ValidationTest & Validation EngineerQualification ProduitTests FonctionnelsTests de Non-RégressionBancs de TestsElectroniqueSystèmes Embarqués.

3 days ago

Quick apply

The best place to find your next move

© 2026. All Rights Reserved.

Talents

Find a job

Create a profile

Solutions and tools