Senior Validation Engineer

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Lead CQV for automation and IT in pharma capital projects, ensuring GMP compliance.
7 days ago ago
Expert & Leadership (13+ years), Experienced (8-12 years)
Contractor
Cork, County Cork, Ireland
Onsite
Role
What you would be doing
compliance
risk assessment
commissioning
validation plans
cqv lead
team collaboration

The successful candidate will be instrumental in ensuring that all systems, equipment, and processes comply with regulatory requirements while supporting the seamless transition from construction to fully validated production environments.

  • Ensure compliance with industry regulations (GMP, FDA, EMA) and company quality standards.
  • Conduct risk assessments, gap analyses, and remediation planning.
  • Provide technical expertise in commissioning and qualification (C&Q) activities, ensuring efficient project delivery.
  • Develop and execute validation plans, protocols (IQ, OQ, PQ), and reports.
  • Lead CQV activities for automation and IT aspects of capital projects.
  • Collaborate with cross-functional teams, including Engineering, Quality, and Operations, to drive validation strategies.
What you bring
bachelor's
cqv
automation
validation
pharma
stakeholder management

If you are an experienced CQV Engineer looking for an opportunity to be at the forefront of pharmaceutical innovation, apply now to be part of these transformative projects.

CQV, Commissioning, Qualification, Validation, Pharma, Biotech, Life Sciences, GMP, FDA, EMA, Automation, IT Systems, Validation Engineer, Laboratory Equipment, Risk Assessment, Process Validation, Capital Projects, Ireland, Manufacturing Expansion, Compliance, Engineering, Project Delivery, Pharmaceutical Industry, Quality Assurance, IQ, OQ, PQ, C&Q

  • Bachelor's degree in Engineering, Computer Science, or a related technical field.
  • Excellent communication and stakeholder management skills, with the ability to present technical findings effectively.
  • Hands-on experience with automation and IT systems used in pharmaceutical manufacturing.
  • Strong knowledge of validation principles, including laboratory analytical instrument qualification.
  • Extensive experience in CQV roles within the Pharmaceutical, Biotech, or Life Sciences sector.
Benefits
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Training + Development
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Interview process
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Visa Sponsorship
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Security clearance
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Your recruiter
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  • Born from a vision to transform how major‑project teams are staffed, Eng Bauen blends deep research with hands‑on networks to support capital projects around the world.
  • From a single mission it has grown into a research‑driven, socially‑connected consultancy operating across EMEA, APAC and the Americas.
  • The firm generates revenue through tailored resourcing services—contract placement, recruitment process outsourcing, direct hire and turnkey project staffing.
  • Over its history, it has supported projects spanning greenfield builds, brownfields, turnarounds and commissioning across sectors such as pharma, energy, infrastructure and manufacturing.
  • Typical engagements include mobilising project management, project controls, construction and engineering experts from FEED through commissioning.
  • Frequently active on high‑value projects—from underground rail upgrades and power‑grid enhancements to complex biotech and pharmaceutical facilities.
  • Stand‑out: its truly borderless mobility support ensures visa, payroll, tax and compliance are handled seamlessly for remote or international deployments.
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