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Catalyx is seeking an IT Validation Specialist join our team and work on our customer site in Cork.
Who We Are:
Catalyx specializes in the science of operational processes. With a footprint across North America and Europe, the company carefully automates and services R&D, production, packaging, and delivery processes—globally—with a sophisticated blend of products, technologies, and lifecycle services. The company was formed in 2022 after CXV Global (Crest Solutions, Xyntek, and VistaLink) and Panacea Technologies joined forces. For over three decades, Catalyx’s partnership-based culture has helped organizations in production-intense, highly regulated industries optimize their operational efficiency, performance, and safety. To learn more about the company's experience and comprehensive suite of capabilities and solutions, visit www.catalyx.ai.
The Role:
Catalyx is a trusted partner in delivering world-class lifecycle services to regulated and high-risk end markets. With a relentless commitment to innovation and excellence, we partner with life science and other highly regulated organisations, to empower them to enhance efficiency, and drive success. As part of this commitment, we are continuously developing our on-site teams to support the advancement of customer operations.
We are seeking an experienced IT Validation Specialist to join our team working within the pharmaceutical sector. This role is critical in ensuring that all IT systems and software comply with regulatory standards, operational requirements, and industry best practices. The ideal candidate will have a strong background in IT Infrastructure, computer system validation (CSV) and regulatory compliance with prior experience in a pharmaceutical or highly regulated environment.
Responsibilities:
* Manage the qualification of IT systems, including hardware, software, and infrastructure within a GMP lab setting.
* Validate software applications used in manufacturing, quality control, and other pharmaceutical processes.
* Collaborate with software vendors to ensure system validation documentation is complete and accurate.
* Manage the lifecycle of validated software, including upgrades and decommissioning.
* Perform periodic reviews of validated systems to ensure continued compliance.
* Develop and maintain traceability matrices to ensure alignment with user requirements.
* Develop and execute validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
* Author, review and approve validation documentation, including validation plans, reports, and risk assessments.
* Ensure all validation activities comply with regulatory standards such as GxP, FDA 21 CFR Part 11, and EMA
* guidelines
* Prepare validation summaries, deviation reports, and corrective/preventive action (CAPA) plans.
Skills and Experience:
* Bachelor’s degree in Computer Science, Information Technology, or a related field.
* 3+ years of experience in IT validation, preferably in a pharmaceutical or regulated environment.
* In-depth knowledge of GxP regulations, FDA 21 CFR Part 11, and other relevant standards.
* Experience with validation of ERP, LIMS, MES, and other pharma-specific IT systems.
* Strong understanding of software development lifecycle (SDLC) and validation best practices.
* Familiarity with IT infrastructure, database management, and networking in a validated environment.
* Excellent problem-solving, analytical, and organizational skills.
* Strong written and verbal communication skills, with the ability to present validation results to diverse audiences.
Why Join Catalyx?
At Catalyx we understand that our people are our greatest asset. For this reason and many others, we take care of them. The team in Catalyx benefits from a Total Rewards package. This includes great personal benefits and professional growth opportunities.
Catalyx is an Equal Opportunity Employer. We are committed to creating a diverse and inclusive workplace where all individuals are valued, respected, and supported. We do not discriminate on the basis of race, colour, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age, disability, veteran status, genetic information, or any other characteristic protected by applicable law. We encourage applications from all qualified candidates, regardless of background, and strive to create a welcoming environment for everyone.
At Catalyx, we are committed to attracting the best global talent. We proudly support our international employees by offering assistance with Critical Skills Visa applications for eligible candidates.
Seniority level
* Seniority level
Not Applicable
Employment type
* Employment type
Contract
Job function
* Job function
Information Technology
* Industries
Automation Machinery Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
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