Computer Systems Validation Engineer

About the Company:

Innopharma Technical Services, part of Innopharma Group, specialises in the training and employment of highly skilled, project-ready, Engineers & Scientists to the (Bio) Pharmaceutical and MedTech Manufacturing Sector.

Location: Dublin & Limerick

Are you ready to take the next step in your career within a leading biopharma environment?

We are now seeking a Computer Systems Validation Engineer to join our team to provide support in validation/qualification activities to our Multinational Manufacturing client based in Co. Limerick.

About the position: This position uses policies and procedures to validate/qualify computer systems, including process automation systems, IS applications/infrastructure, and enterprise systems. Plans, coordinates, and participates in a compliant validation process for quality information technology and automation systems which require formal validation documentation under appropriate regulatory requirements and company manufacturing standards.

Key Responsibilities:

• Prepares and reviews validation documentation for projects and change controls.
• Manages change controls, non-conformances, and other compliance-related tasks.
• Reviews and contributes to current and future CSV procedures and policies.
• Analyses test results against acceptance criteria to determine compliance.
• Investigates, troubleshoots, and recommends solutions or improvements.
• Identifies current and future compliance requirements and proposes methods for implementing and maintaining necessary procedures, actions, and documentation.
• Coordinates validation activities with internal departments and external vendors/contractors.
• Supports regulatory audits and communicates company computer validation policies.
• Assesses computer systems for Part 11 and Annex 11 compliance gaps.
• Manages projects and prepares progress reports using Microsoft Project and other tools.
• Supervises, leads, or manages junior personnel as required.

Preferred Experience:

• Minimum BS/BA in Engineering, Chemistry, or Life Sciences is required.
• 3+ years of related experience within the fields of Automation and Computer systems and IT
• Infrastructure Qualification/validation is desired; will substitute relevant experience for education.
• Experience in a GMP environment is essential.
• Strong technical writing and documentation skills.
• Excellent communication and collaboration skills.
• A proactive, detail-focused approach with a passion for continuous improvement.

Note:
•Due to the nature of the business additional duties may be assigned from time to time.
•All applicants must be eligible to work in Ireland.

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If you’re passionate about manufacturing excellence and eager to grow in a fast-paced, regulated environment, we want to hear from you.

Apply Now