The Quality Systems Specialist is responsible for ensuring compliance with Good Manufacturing Practice (GMP) and regulatory standards. This role involves managing quality systems, supporting facility projects, conducting training, performing audits, and maintaining documentation for products manufactured in the Dublin facility.

The Qualified Person is responsible for the release of Nutrition, Chemo, and Antibiotic products, ensuring compliance with regulatory standards and procedures. Responsibilities include managing quality assurance, overseeing the compounding process, and supporting facility projects while ensuring adherence to Good Manufacturing Practice (GMP) and corporate standards.