CQV Engineer – Sterile Drug Product Facility
Location: Dublin
Sector: Biopharmaceutical Manufacturing
Type: Contract| On-Site
We are currently recruiting on behalf of a leading pharmaceutical company in Dublinfor an experienced CQV Engineer to support the commissioning, qualification, and validation (CQV) of equipment and utilities within a Sterile Drug Product (SDP) facility.
Key Responsibilities:
* Develop and execute CQV protocols in line with GMP and global procedures
* Ensure commissioning and validation of both GMP and non-GMP systems
* Lead FATs and integrate testing results into qualification strategies
* Manage deviations and implement risk mitigation plans
* Collaborate with multidisciplinary teams to deliver projects safely, on time, and within budget
* Support training, documentation, and project execution for all assigned systems
* Act as designee for the CQV Lead when required
Your Experience:
* Minimum 5 years in pharmaceutical CQV, ideally within sterile drug product environments
* Proven expertise with equipment such as Single Use Mixers, TCUs, TFFs, Utility Panels, Autoclaves, Parts Washers, and Powder Handling Systems
* Experience with integrated automation systems in pharma manufacturing
* Strong background in project documentation, testing execution, and compliance
* Degree (BSc/BEng) in a scientific, technical, or engineering discipline
This role offers a unique opportunity to work in a cutting-edge facility with a focus on safety, quality, and innovation. To apply, please send your CV to jobs@forcerecruitment.com
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