C
C AgentsCQV Engineer
Read straight from C Agents's careers page, verified 23h ago.Seekless can tailor your résumé to it.
Seekless can write your résumé for this posting first.
Before you apply
LocationLimerick
Work modeon-site
Typefull-time
SeniorityMid
DepartmentEurope Life Sciences, North Europe
Company size501–1,000 people
PostedJul 20, 2026 · 3mo ago
Verified live23h ago
May no longer be actively hiring
Posted by the company on Jul 20, 202677% of this company's open roles have been listed for 90+ days
At a glanceSummarised by Seekless from the posting.
Experience in 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
Benefits
Equal opportunity employer
About the 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!
Legal
We are an equal opportunity employer; we are proud to employ veterans and promote a diverse culture in our workplace. Diversity is a strength for our global company. We pledge that CAI will be operated in a way that is fair and equitable to all – our employees, our customers, and the broader society. This job description is not all inclusive and you may be asked to do other duties.