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.
