Were Hiring: Validation Engineer (Onsite Loughrea) Are you looking to grow your career in validation within a dynamic, GMP-regulated environment?
If you enjoy hands-on technical work, solving problems, and contributing to high-quality manufacturing processes, this could be a great opportunity for you.
Were seeking a Validation Engineer to support our Validation Team Lead and help drive key validation activities across the site.
This is a full-time onsite role based in Loughrea.
What Youll Be Doing As a Validation Engineer, you will play an important role in ensuring our validation systems are compliant, robust, and well-documented.
Your responsibilities will include: 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.
24 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.
If youre detail-oriented, motivated, and eager to build your expertise in validation, wed love to connect with you.
Ready to take the next step?
Apply or reach out for a confidential conversation!
#LI-EB6 Skills: GMP Compliance Validation Expertise Strong Documentation Analytical Skills Team Collaboration Benefits: Bonus