CQV Engineer (Pharmaceutical)

TL;DR

CQV Engineer (Pharmaceutical): Supporting the execution of validation protocols and managing CQV activities for pharma manufacturing projects with an accent on safety, quality, and operational standards. Focus on drafting and executing validation protocols and troubleshooting doc prep and execution phases.

Location: Onsite in West Dublin, Ireland

Company

International project delivery company providing project management, process design, and commissioning and qualification services for leading multinational clients.

What you will do

• Manage all CQV activities from initiation and concept through construction to final handover.
• Support project managers in the delivery of a diverse portfolio of projects.
• Identify and apply the appropriate Commissioning and Qualification strategies (IC/IQ and OC/OQ).
• Draft and execute validation protocols to meet client and regulatory expectations.
• Communicate and troubleshoot issues arising during document preparation and execution.
• Assess and manage CQV execution support requirements from vendors and contractors.

Requirements

• Location: Must be based in or able to work onsite in West Dublin, Ireland.
• Third Level Degree in a relevant discipline or equivalent professional experience.
• Minimum 5 years of experience working within a GMP environment as a CQV or Project Engineer.
• Proficiency in project management controls and experience with multi-function projects.
• Strong oral and written communication skills for professional client interaction.

Nice to have

• Experience using the ValGenesis validation platform.

Culture & Benefits

• Employee-owned company culture focused on commitment and drive.
• Strong emphasis on Corporate Responsibility and Sustainability.
• Inclusive workplace committed to diversity, mutual respect, and belonging.
• Fair and accessible hiring process with reasonable accommodations for candidates with disabilities.