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We currently seek for a Validation Engineer to join our Site Validation Team on a permanent basis, reporting directly to the Site Process and Cleaning Validation Lead in AbbVie Westport. As our new Sterilization Validation Engineer, you will be responsible for ensuring that medical devices, pharmaceutical products, and equipment are sterilized effectively and consistently to meet regulatory and quality standards. We perform all validation activities n line with Global Standards, FDA, HPRA and other MOH regulatory requirements.