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Open nowPosted 70 days ago

CQV Engineer

cagents100 open roles

Where
Limerick
Work mode
On site
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Your applicationOpen nowCQV Engineercagents · Limerick

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The clock on this job

Early applications get read.

7.4% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.5%1 day
  2. 3.5%3 days
  3. 7.4%7 days
  4. 13.2%14 days
  5. 34.6%30 days
This job: posted 70 days ago

The posting

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.

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