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 Dublin for 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