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Commissioning engineer

Dublin
Atrium (EMEA)
Commissioning engineer
€80,000 - €100,000 a year
Posted: 24 October
Offer description

Job Overview

Atrium Global is recruiting on behalf of our client, a leading pharmaceutical manufacturer, for an experienced Small Equipment C&Q Engineer to support commissioning and qualification activities at their Cruiserath Drug Product Facility.

Onsite Requirements: This is a site-based role

Engagement Type: LTD Company Contractor

Day Rate / Hourly Rate: Up to €75 per hour (DoE)


RESPONSIBILITIES

* Develop and execute CQV testing documentation for benchtop, mobile, analytical, PAT, incubators, BSCs, and TCU equipment in the sterile drug product facility.
* Deliver on key project objectives, including safety, CQV schedule adherence, and quality of project documentation and electronic records.
* Ensure GMP equipment testing is performed in compliance with company policies, GMP standards, and EU/FDA regulations.
* Conduct commissioning testing in line with project standards and requirements.
* Manage deviations associated with assigned equipment and utilities.
* Apply risk management principles to identify, categorise, and mitigate CQV risks through action plans.
* Execute FAT testing and integrate outcomes into the qualification process.
* Ensure all assigned training is completed on time to meet site compliance metrics.


REQUIREMENTS

* Bachelor’s degree in a scientific, technical, or engineering discipline.
* Minimum 3–5 years of CQV experience within the pharmaceutical industry.
* Proven experience across the CQV project lifecycle — from design through to commissioning, qualification, and handover.
* Experience with CQV of drug substance or drug product small equipment with integrated automation.
* Strong documentation, execution, and planning skills with a track record of on-time delivery.
* Excellent communication and teamwork skills with the ability to work in a matrix environment.
* Experience with electronic validation platforms (e.g. ValGenesis, Kneat).
* Demonstrated ability to execute CQV testing from initiation to completion.
* Familiarity with sterile drug product filling line environments (highly desirable).


Legal Right to Work

Candidates must have the legal right to work in Ireland at the time of application. Sponsorship is not available for this role.

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