Business Manager | UK & EMEA Region | Global Project Execution Expertise
Ireland | Long-term Contract
ENG Bauen has been working closely with our clients, supporting capital projects across the Life Sciences, Pharmaceutical, and Energy sectors. As part of our continued growth, we are seeking skilled professionals to join high-impact projects that are shaping the future of pharmaceutical manufacturing.
We are partnering with a leading pharmaceutical organisation that is making significant investments in cutting‑edge pharmaceutical and biotech manufacturing. As part of its growth strategy, the company is undertaking complex capital expenditure projects at one of its key sites in Ireland. With project values ranging from €50M to €250M, these initiatives are focused on enhancing manufacturing capabilities, expanding production facilities, and advancing life sciences technologies.
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.
The role:
* Lead CQV activities for automation and IT aspects of capital projects.
* Develop and execute validation plans, protocols (IQ, OQ, PQ), and reports.
* Ensure compliance with industry regulations (GMP, FDA, EMA) and company quality standards.
* Collaborate with cross‑functional teams, including Engineering, Quality, and Operations, to drive validation strategies.
* Conduct risk assessments, gap analyses, and remediation planning.
* Provide technical expertise in commissioning and qualification (C&Q) activities, ensuring efficient project delivery.
The Person:
* Bachelor's degree in Engineering, Computer Science, or a related technical field.
* Extensive experience in CQV roles within the Pharmaceutical, Biotech, or Life Sciences sector.
* Strong knowledge of validation principles, including laboratory analytical instrument qualification.
* Hands‑on experience with automation and IT systems used in pharmaceutical manufacturing.
* Excellent communication and stakeholder management skills, with the ability to present technical findings effectively.
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
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Manufacturing, Engineering, and Consulting
Industries
Pharmaceutical Manufacturing, Engineering Services, and Automation Machinery Manufacturing
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