Validation Engineer

A leading Pharmaceutical / MedTech manufacturing company are seeking an experienced Validation Engineer to join their team on a 6-month contract to support a decommissioning project at their Dublin site.

This role will be heavily focused on validation documentation and reporting, including the creation, execution, and completion of all required validation deliverables associated with equipment and/or system decommissioning in a regulated environment. The successful contractor will be comfortable working with a high level of autonomy and operating in a predominantly onsite, days-based role.

Key Responsibilities

• Support validation activities related to a decommissioning project
• Author, review, and execute validation documentation, including but not limited to:
• Decommissioning plans and protocols
• Validation reports
• Traceability matrices
• Ensure all validation activities are compliant with GMP and regulatory requirements
• Liaise with cross-functional teams (Engineering, QA, Manufacturing) as required
• Ensure documentation is completed accurately, on time, and to a high standard
• Provide validation input and technical expertise throughout the project lifecycle

Required Experience & Skills

• 4–5+ years’ experience working as a Validation Engineer
• Background in Pharmaceutical, xcfaprz MedTech, or other highly regulated industries
• Previous experience supporting decommissioning, equipment lifecycle, or similar validation projects
• Strong experience with validation documentation and report writing
• Good understanding of GMP, regulatory, and quality standards
• Ability to work independently with minimal supervision
• Strong attention to detail and documentation accuracy