We are partnering with a leading global life sciences company that is currently constructing a €330-million, state-of-the-art biopharmaceutical facility in County Kerry. This cutting-edge, greenfield plant is designed to the highest environmental and sustainability standards and will focus on the aseptic fill-finish and lyophilization manufacturing of advanced biologics (including mAbs and ADCs).
As a CQV Engineer, you will join the project during a critical phase of construction, commissioning, and validation. This is a long-term contract offering the opportunity to work with next-generation biotechnology equipment and play a key role in building a facility from the ground up.
Key Responsibilities
- Execution: Author, review, and execute CQV lifecycle documentation (including URS, FMEA, DQ, IQ, OQ, and PQ protocols) for clean utilities, process equipment, and automated systems.
- System Ownership: Take technical ownership of assigned systems, ensuring compliance with global regulatory standards (FDA, EMA) and ASTM E2500 principles.
- Vendor Management: Partner with design teams and vendors during Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT).
- Cross-Functional Collaboration: Work closely with Construction, Engineering, Quality Assurance, and Operations teams to ensure seamless system handovers.
- Troubleshooting: Identify, investigate, and resolve protocol deviations, implementing robust corrective and preventive actions (CAPAs).
Requirements & Qualifications
- Education: Bachelor's degree in Engineering, Biotechnology, Chemistry, or a related scientific discipline.
- Experience: 3+ years of dedicated CQV engineering experience within the biopharmaceutical or pharmaceutical sector.
- Technical Expertise: Strong background in aseptic processing, sterile fill-finish, compounding, or lyophilization technologies is highly desirable.
- Utility & Equipment Knowledge: Familiarity with clean utilities (WFI, Clean Steam, Purified Water) and process cleanroom environments.
- Regulatory Knowledge: Deep understanding of EU/FDA GMP regulations, Annex 1, data integrity principles, and risk-based validation approaches.
- Soft Skills: Excellent technical writing skills, a proactive attitude toward safety and problem-solving, and the ability to adapt to a fast-paced greenfield project environment.
