CSV Engineer

About Catalyx

Catalyx is a machine vision and automation business that combines technology and people to help manufacturers and logistics organisations improve quality and throughput at scale. With more than 30 years of experience, 9 offices worldwide, over 550 employees, and 3,000+ completed projects, the company delivers technical expertise and new technology applications for highly regulated industries. More information is available at the company website.

Role overview

Catalyx is hiring a CSV Engineer for a major pharmaceutical assignment in Cork, supporting laboratory systems and quality control operations within a GMP-controlled setting. The position covers both current and upcoming laboratory initiatives, with a strong emphasis on laboratory IT, validation work, documentation, and support across multiple functions. You will partner with QC, IT, engineering, and project teams to help ensure laboratory systems stay compliant, dependable, and aligned with regulatory and data integrity expectations. This is a hybrid-style role with exposure to a variety of laboratory systems and digital transformation activities across the site.

Key responsibilities

• Contribute to laboratory systems projects in a GMP-regulated quality control environment.
• Coordinate with site teams on requirements capture, configuration specifications, and IOQ protocol preparation.
• Draft, assess, and sign off validation and lifecycle records for laboratory systems.
• Help with risk assessments connected to laboratory systems and related workflows.
• Assist with deployment tasks, system setup, and support/training for end users.
• Support fault finding and the ongoing stability of QC laboratory IT platforms.
• Work across QC, IT, engineering, validation, and project groups to keep delivery moving.
• Help maintain GMP compliance, data integrity, and regulatory expectations, including principles linked to 21 CFR Part 11.
• Take part in continuous improvement efforts within the laboratory systems space.
• Keep documentation thorough and ensure work is completed to a high compliance standard.

Candidate profile

The ideal candidate will have a degree in IT, Computer Science, Business Information Systems, Chemistry, Biology, or a related subject. Prior exposure to laboratory systems or GMP systems in a pharmaceutical or regulated environment is an advantage. A strong working knowledge of Microsoft Windows, including Windows 10/11 and server-based environments, is required. Experience with CSV, system lifecycle records, or qualification activities is helpful. You should understand GMP settings, data integrity, and regulatory compliance principles, along with strong troubleshooting ability. Clear communication, stakeholder handling, the ability to work both independently and in cross-functional teams, and excellent organisation across multiple priorities are all important. Experience supporting QC laboratory operations or laboratory applications is desirable.

Why join

Catalyx offers a Total Rewards package with personal benefits and opportunities for professional growth. The company is committed to an inclusive, diverse workplace and encourages applications from all qualified candidates. For eligible international hires, support is available for Critical Skills Visa applications.

Equal opportunity

Catalyx maintains an equal opportunity hiring approach and does not discriminate on the basis of race, colour, religion, sex, pregnancy, gender identity, sexual orientation, national origin, age, disability, veteran status, genetic information, or any other protected characteristic.