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Job Summary
Our client are a leading pharmaceutical company who are hiring a QA Validation Engineer to join their team in Dublin. This job would be supporting several ongoing projects and their associated validation activities, specifically review and approval of validation documentation. Please note that this will be a contract position.
Main Duties
As QA Validation Engineer, your job will be to ensure the validation and quality assurance of site equipment, utilities, processes and software in compliance with policies and standards.
Conducting risk assessments of equipment modifications and new equipment introductions.
Preparing and executing validation documents.
Carrying out reviews of GMP manufacturing equipment to ensure compliance.
Providing validation support to various groups across the site to enable changes.
Any other duties as required.
Your background
For this QA Validation Engineer job, you will have 3+ years’ experience in a similar position within the pharmaceutical or medical device sectors.
You will also have a relevant third level degree.
Why Join Arcadis?
At Arcadis, we empower individuals to excel because your contributions matter. Taking a skills-based approach, we provide opportunities for you to shape your career, maximize your impact, and grow professionally.
By joining us, you’ll engage in meaningful work that drives sustainable solutions for a better planet while leaving a lasting legacy.
Our Commitment to Equality, Diversity, and Inclusion
We are dedicated to creating an environment where everyone can thrive. Through our six ED&I workstreams—Age, Disability, Faith, Gender, LGBT+, and Race—we foster innovation by bringing together diverse perspectives. Together, we strive to improve quality of life while building a more inclusive future.
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