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, you'll 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
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