This is a fantastic opportunity to join a high-impact programme with one of the most established and globally recognised pharmaceutical companies in the world. You will play a key role in ensuring software and systems are validated in line with strict regulatory standards. The initial contract is for 12 months, with good potential for extension, offering long-term contracting opportunities in a high-growth, life sciences environment.

kill Set-Skill Set:
Veeva Vault, Oracle, SQL Server, and Jira. Industry exp: Life Sciences

Validation Specialist for an initial 12-month contract based in Cork.What you’ll do:

Lead and support validation and testing processes in line with SDLC methodologies
Create and execute validation plans, protocols, and reports
Ensure regulatory compliance through comprehensive documentation and risk management
Analyse data and manage documentation using tools such as Veeva Vault, Oracle, SQL Server, and Jira
Collaborate with cross-functional teams to deliver compliant and high-quality solutions
Maintain and update validation documentation and reports to meet ongoing compliance requirements

The skills you’ll need:
Proven experience in validation and software testing processes
Strong documentation skills, including authoring validation plans and protocols
Familiarity with regulatory frameworks and compliance in the Life Sciences sector
Hands-on experience with tools such as Veeva Vault, Oracle, SQL Server, and Jira
Solid understanding of the Software Development Lifecycle (SDLC)