About this role
Are you an experienced CQV Engineer looking to join a dynamic project team delivering complex pharmaceutical or life sciences projects?
We are seeking a driven and collaborative CQV professional to support commissioning, qualification and validation activities across a range of GMP regulated systems, facilities and equipment. This is an excellent opportunity to work on high impact projects in a fast paced and technically challenging environment.
Key Responsibilities
Execute Commissioning, Qualification and Validation (CQV) activities in line with project schedules and GMP requirements.
Support commissioning, startup and qualification of equipment, utilities and process systems.
Prepare, review and execute validation documentation including protocols, reports, and traceability matrices.
Lead or participate in design reviews, FATs, SATs, commissioning, IQ, OQ and PQ activities.
Manage qualification documentation through the full CQV lifecycle.
Coordinate activities with engineering, operations, quality, contractors and equipment vendors.
Track progress, identify risks and support timely project delivery.
Assist with change controls, deviations, punch lists and documentation management.
Ensure all activities are performed to the highest safety and compliance standards.
Provide technical support during project execution and system handover
What We're Looking For
Experience within Pharmaceutical, Biotechnology, Medical Device or Life Sciences industries.
Background in Commissioning, Qualification, Validation, Engineering or Technical Operations.
Understanding of GMP and regulated manufacturing environments.
Experience working with equipment, process systems, clean utilities, facilities or automation systems.
Strong documentation, problem-solving and stakeholder engagement skills.
Ability to work effectively as part of a multidisciplinary project team.
Why Apply?
Opportunity to work on industry-leading projects
Exposure to cutting-edge manufacturing technologies
Collaborative and supportive team environment
Competitive salary or contract rates available
Potential for long-term career progression
Interested in learning more? Apply today!
Frequently Asked Questions
Is the salary disclosed for the CQV Engineer position at cagents?
The salary for this CQV Engineer role at cagents is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the CQV Engineer position at cagents located?
This CQV Engineer role at cagents is based in Dublin. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the CQV Engineer role at cagents full-time or part-time?
This is listed as a Full Time position. It is posted as a CQV Engineer role in the North Europe department at cagents.
Which team or department does the CQV Engineer at cagents belong to?
This CQV Engineer position is part of the North Europe department at cagents. See the full job description for more information about the team structure and responsibilities.
How do I apply for the CQV Engineer position at cagents?
Click the "Apply Now" button on this page. You will be redirected to cagents's official application portal hosted on lever where you can submit your application directly.
When was the CQV Engineer job at cagents posted?
This CQV Engineer position at cagents was posted on Jul 20, 2026. Apply as soon as possible โ early applications are often reviewed first.