# CQV Engineer at CAI

CQV Engineer at CAI in Limerick. On-site, full-time. Posted July 20, 2026.

- Company: CAI
- Location: Limerick
- Workplace: On-site
- Job type: Full-time
- Posted: 2026-07-20
- Apply: https://jobs.lever.co/cagents/66c8603b-0a79-4a18-a1c8-962a01888327/apply
- Source: https://jobmagic.ai/jobs/cqv-engineer-cai-fwn1ny

## Requirements

- 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.

## Description

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!
 
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.