Job Title: Validation Engineer Location: Galway Status: Permanent Position Summary: This is an exciting opportunity to contribute to a growing, collaborative environment where your expertise helps drive operational excellence and regulatory compliance.
Reporting to the Validation Team Lead, youll help implement the Validation Master Plan, maintain SOPs, execute validation activities across processes, cleaning, equipment, analytical instruments and utilities.
Key Responsibilities: Maintain accurate, audit-ready validation documentation in line with SOPs and regulatory requirements Ensure all validation activities comply with GMP, regulatory guidelines, and internal procedures.
Collaborate closely with manufacturing, quality, engineering, and analytical teams to coordinate validation activities.
Support technology transfers and new product introductions through effective validation planning and execution.
Qualifications and Requirements: Strong knowledge of GMP and validation principles.
2+ years experience in validation within a GMP-regulated environment Ability to maintain audit-ready records and ensure accuracy and completeness in validation documentation.
Degree in Engineering, Pharmaceutical Science, or a related discipline For a confidential conversation about the position contact Karl on or By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment purpose