Job Title
Validation Engineer (Onsite – Loughrea)
Location
Loughrea, Ireland
Employment Type
Full-time
Seniority Level
Mid-Senior level
Job Function
Pharmaceutical Manufacturing
What You'll Be Doing
Developing, executing, and documenting validation protocols and reports across process, cleaning, equipment, analytical instruments, and utilities.
Ensuring all validation activities align with GMP requirements, regulatory guidelines, and internal procedures.
Supporting technology transfers and new product introductions through well-planned validation work.
Maintaining accurate, complete, and audit-ready validation documentation.
Assisting with updates and implementation of validation-related SOPs under the guidance of the Validation Team Lead.
Contributing to internal and external audit readiness.
Identifying opportunities to improve validation processes and enhance operational efficiency.
Collaborating closely with manufacturing, quality, engineering, and analytical teams to coordinate validation efforts.
Providing technical support during investigations and troubleshooting activities.
What You Bring
A degree in Engineering, Pharmaceutical Science, or a related field.
2–4 years
of experience in validation within a GMP-regulated environment.
Experience with process, cleaning, and equipment validation is preferred.
Skills That Will Help You Succeed
Solid understanding of GMP and core validation principles.
Exceptional documentation accuracy and attention to detail.
Strong organizational skills and the ability to manage multiple tasks.
A collaborative mindset and the ability to work effectively across functions.
Strong troubleshooting and problem-solving abilities.
Commitment to quality, compliance, and continuous improvement.
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Ready to take the next step?
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