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Process Engineer (CQV)
DPS Engineering (Netherlands) B.V.
About the role
Submit Your Resume CV Job Search Graduate Opportunities Submit Your Resume CV Job Search Graduate Opportunities Process Engineer (CQV) Location: West Dublin Employment Type: Full-Time Date Posted: 23/Sep/2026 Apply for this job Overview Our Client is seeking a Process Engineer to support capital projects on site, providing technical oversight of Commissioning, Qualification and Validation (CQV) activities. The successful candidate will ensure process requirements, GMP principles and risk-based methodologies are appropriately applied throughout project delivery, maintaining compliance and inspection readiness.
What you'll do
Provide technical oversight and review of CQV documentation, including commissioning plans, risk assessments, qualification protocols and reports. Ensure process requirements are effectively translated into GMP-compliant design and qualification strategies. Support the identification, justification and control of critical quality attributes (CQAs) and critical process parameters (CPPs). Apply risk-based approaches to determine qualification scope, testing requirements and verification activities. Review and approve CQV strategies, plans and lifecycle documentation. Challenge and guide project teams, vendors and CQV service providers to ensure regulatory and industry best practice compliance. Support design reviews, change controls and deviation investigations from a technical compliance perspective. Ensure systems remain in a validated state and support ongoing inspection readiness.
What you'll bring
Bachelor's degree in Engineering (Chemical, Mechanical, Electrical or related discipline). Minimum 5 years' experience in Commissioning, Qualification and Validation (CQV) within a regulated pharmaceutical environment. Strong understanding of pharmaceutical manufacturing processes, CQAs and CPPs. Working knowledge of GMP regulations and industry standards, including EU GMP, FDA and ICH guidelines. Experience reviewing and approving CQV lifecycle documentation. Strong risk assessment, problem-solving and analytical skills. Excellent stakeholder management and communication abilities. Ability to identify, assess and escalate compliance and quality risks.