---
title: 'CQV Lead at CAI'
canonical: 'https://feeny.ai/job/cqv-lead-cai-limerick-e0tx4s64qg0j'
type: 'job'
last_seen: '2026-10-14'
---

# CQV Lead at CAI

- **Company:** CAI
- **Location:** Limerick, Ireland
- **Employment:** full-time
- **Work type:** onsite
- **Posted:** 2026-10-06
- **Last confirmed live:** 2026-10-14
- **Apply:** https://jobs.lever.co/cagents/1436387b-9dc4-414e-83b5-614a8b1507e2

## Job description

We are seeking an experienced CQV Lead to drive qualification and validation activities for a broad range of laboratory and benchtop equipment within a GMP-regulated environment. This position offers the opportunity to lead critical qualification projects, work closely with Quality, Engineering, Validation, and Laboratory teams, and play a key role in supporting both operational excellence and regulatory compliance. The successful candidate will provide technical leadership across the full equipment lifecycle, from installation and qualification through ongoing compliance and continuous improvement initiatives.

## Key Responsibilities

Lead commissioning, qualification, and validation activities for laboratory and benchtop equipment within GMP environments. Develop and execute qualification documentation, including IQ, OQ, PQ protocols and final reports. Support the introduction of new laboratory equipment and technologies, ensuring compliance with internal procedures and regulatory requirements. Coordinate qualification activities with Quality, Operations, Laboratory, Engineering, and external vendors. Manage deviations, change controls, CAPAs, and investigations related to qualified equipment. Ensure equipment remains in a validated state through periodic reviews, requalification activities, and lifecycle management. Provide technical guidance and mentorship to CQV engineers and validation team members. Support internal and external audits and regulatory inspections. Identify and implement process improvements to enhance qualification efficiency and compliance.

## What We're Looking For

Degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or a related discipline. Experience leading CQV or validation activities within pharmaceutical, biotechnology, or medical device manufacturing. Strong knowledge of GMP requirements and qualification lifecycle principles. Hands-on experience qualifying laboratory and benchtop equipment such as: HPLC, UPLC and chromatography systems TOC analyzers UV-Vis spectrophotometers Autoclaves and sterilization equipment Incubators and environmental chambers Balances and weighing systems Freezers, refrigerators and stability chambers Particle counters and laboratory instrumentation Experience authoring and reviewing qualification protocols and reports. Strong stakeholder management and project leadership skills. Excellent communication and problem-solving abilities. Other Requirements This is a site based role Eligible to work in the EU without the need for visa sponsorship, now or in the future. What Success Looks Like You will be the go-to CQV subject matter expert for laboratory equipment qualification, ensuring projects are delivered on schedule while maintaining the highest standards of quality, compliance, and inspection readiness. Why CAI? At CAI, our people are at the heart of everything we do. We partner with the world's leading life sciences companies to deliver innovative projects that ultimately improve patient lives. You'll work alongside industry leading experts in a collaborative environment that supports professional growth and technical excellence.

If you're a CQV professional looking to contribute to a challenging pharmaceutical project while developing your career with a global consultancy, we'd love to hear from you.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

## About CAI

## Company Overview
- **One-liner**: CAI is a global professional services firm that accelerates operational readiness and excellence for life sciences and mission-critical facilities through commissioning, validation, engineering, and digital transformation expertise.
- **Entity Type**: Private (Privately Held; raised a venture round in May 2026)
- **Headquarters**: Indianapolis, Indiana, United States
- **Founded**: 1996
- **Founders**: Not publicly available

## Core Business
- **Primary industry/industries**: Life Sciences (pharmaceutical, biotech, medical device manufacturing) and Mission Critical (data centers, high-tech facilities)
- **Target customers**: B2B – enterprise-level pharmaceutical companies, biotech firms, data center operators, and regulated manufacturers
- **Mission or purpose statement**: “Making what’s next possible” by delivering precision, efficiency, and innovation through commissioning, qualification, validation, and operational readiness services.

## Products & Services
For each major offering:
- **Commissioning & Qualification (C&Q)**: End-to-end commissioning and qualification services for new and modified facilities, ensuring regulatory compliance and operational readiness.
- **Validation Services**: Computer Systems Validation (CSV), cleaning validation, process validation, and equipment validation for life sciences clients.
- **Automation & Digital Transformation**: Automation engineering, digital twin solutions, and technology integration to improve facility performance and data integrity.
- **Building Commissioning**: Mechanical, electrical, and plumbing commissioning for mission-critical buildings, including data centers and commercial facilities.
- **Human Performance & Operational Excellence**: Consulting and training programs to reduce human error, improve safety, and optimize asset management.
- **Project Management**: Owner’s project management and full-scale operations support for complex capital projects.

## Market Standing
- **Valuation/Market Cap**: Not disclosed (private)
- **Key Metric**: Annual Revenue of ~$10.2M (as of latest available data); Total Funding – venture round raised in May 2026 (amount undisclosed, 1 investor)
- **Notable Investors/Partners**: One venture investor (May 2026 round); strategic partnerships with technology vendors (unspecified) and participation in industry bodies such as ASHRAE, ASTM, BCA, and ISPE.
- **Growth Signals**: 
  - Employee headcount of 562, up 2.6% YoY
  - LinkedIn followers surged 72.3% over the past year, indicating strong brand interest
  - 84 active job postings globally
  - Offices in 5 countries (US, Ireland, Singapore, China, Australia) and operations across 21 countries
  - Clients include top pharma firms (Pfizer, Eli Lilly, MSD, Novartis, Thermo Fisher Scientific)

## Competitive Advantages
- **30 years of deep domain expertise** in highly regulated environments, giving CAI a track record that few competitors can match.
- **Elite, credentialed talent** – team members are active in nearly 30 professional societies and help set industry standards (ASHRAE, ISPE, ASTM, BCA).
- **Global footprint with local delivery** – ability to support multinational clients across the US, Europe, and Asia-Pacific.
- **End-to-end lifecycle support** – from commissioning and validation to digital transformation and operational excellence – reducing handoff risks.
- **Strong alumni pipeline to/from top pharma** – CAI attracts talent from Pfizer, Eli Lilly, Bristol Myers Squibb, and others, signaling deep industry credibility.

## Strategic Focus
- **Investing in Digital Transformation** – leveraging digital twin technology and automation to drive efficiency for clients.
- **Expanding Mission Critical Services** – actively hiring Data Center Commissioning Project Managers and Engineers in the US and Europe.
- **Sustainability Integration** – weaving green building practices (LEED, Net Zero Energy) into all client engagements.
- **Talent Development** – emphasizing top-tier training and career progression to retain high-knowledge employees.

## Why Work Here
- **Culture of teamwork and continuous improvement** – employee testimonials highlight a supportive team environment and commitment to process excellence.
- **Global, varied projects** – work on high-impact projects for leading pharma and data center clients across 21 countries.
- **Clear career growth** – career/professional development opportunities, exposure to multiple disciplines (validation, automation, commissioning, human performance).
- **Benefits package** – comprehensive health insurance, paid time off, competitive 401(k) contribution, income protection, and additional local-region benefits.
- **Remote/hybrid/office policy** – roles vary; many positions are client-site based (e.g., commissioning engineers travel to data centers or manufacturing sites). Some office locations available.
- **Engineering culture** – strong focus on quality, problem-solving, and precision; ideal for engineers, validation specialists, and project managers who thrive in regulated environments.

## Sources
1. [caiready.com](https://caiready.com/) – Company homepage and about page
2. [caiready.com/about](https://caiready.com/about/) – Company history and mission
3. [caiready.com/careers](https://caiready.com/careers/) – Careers page with benefits and culture
4. [linkedin.com/company/caiconnected](https://linkedin.com/company/caiconnected) – LinkedIn company profile and employee data
5. [jobs.lever.co/cagents](https://jobs.lever.co/cagents) – Active job postings

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