- Our ClientOur client is a leading animal pharmaceutical company based in County Wicklow. POSITION SUMMARYThis position will report directly to the Rathdrum Site Quality Operations (QO) Lead and will serve as partners alongside other stakeholders to ensure compliance and execution of site operational activities and ensure the site is permanently inspection ready. The Rathdrum QA Specialist-Operations will have responsibility for ensuring that the process fOur ClientOur client is a leading animal pharmaceutical company based in County Wicklow. POSITION SUMMARYThis position will report directly to the Rathdrum Site Quality Operations (QO) Lead and will serve as partners alongside other stakeholders to ensure compliance and execution of site operational activities and ensure the site is permanently inspection ready. The Rathdrum QA Specialist-Operations will have responsibility for ensuring that the process f
- ResponsibilitiesEnsure training documentation is current and accessible.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global teams to meet documentation and compliance needs.Lead or support continuous improvement initiatives and operational technology improvements.ResponsibilitiesEnsure training documentation is current and accessible.Author and review technical documents, including SOPs, protocols, and reports.Provide support and troubleshooting for systems; assist with deviations, investigations, and change controls.Collaborate across departments, external vendors, and global teams to meet documentation and compliance needs.Lead or support continuous improvement initiatives and operational technology improvements.
- ResponsibilitiesManage the key Quality Systems for the site (Veeva Vault, LMS).Oversee preparation, approval, and training upload of site documentation (GMP, EHS, operational procedures) in Veeva Vault and LMS.Track site documentation schedule, escalate issues, and support timely resolution.Administer LMS and ensure training documentation is accessible.Coordinate records retention and manage control of all records through the Records Management process/tooResponsibilitiesManage the key Quality Systems for the site (Veeva Vault, LMS).Oversee preparation, approval, and training upload of site documentation (GMP, EHS, operational procedures) in Veeva Vault and LMS.Track site documentation schedule, escalate issues, and support timely resolution.Administer LMS and ensure training documentation is accessible.Coordinate records retention and manage control of all records through the Records Management process/too
