Validation Engineer

We are looking for a Validation Engineer to join a Pharmaceutical Company in Dublin. This is a 12 month hourly rate contract position.

Requirements:

• Generate and review a variety of manufacturing and inspection equipment validation deliverables, including: protocols, reports, specifications, manuals, work instructions, procedures, qualifications (IQ, OQ, PQ), engineering studies (Process Development, confirmation or exploratory studies) and production documentation.
• Adhere to Quality Management Systems (QMS) and Good Documentation Practices (GDP) to ensure all records are accurate, error-free, and audit-ready.
• Consult with subject matter experts and stakeholders to gather data, determine requirements, and manage documentation flow across multiple simultaneous projects.
• Support Lean Sigma initiatives and maintain engineering records within document control software to ensure version integrity and procedural continuity.
• Author, edit, and review high-quality validation deliverables, including IQ/OQ/PQ protocols, engineering studies, work instructions, and technical reports.
• Initiate and support intra and internal department meetings and projects to achieve team goals.

Skills, Attributes, Experience:

• Minimum 5+ years experience in Validation/Process Engineering ideally with a background in Pharmaceuticals or Medical Device.
• Bachelor's Degree in Engineering or a related technical field.
• Support and contribute in Lean Sigma programs and activities towards delivery of the set target.
• Has superior analytical, organizational, leadership and technical skills.
• Excellent interpersonal skills: good team player and individual contributor as well.
• Interpret data, read and write, effective communication, decision making, presentation skills.