To ensure that Vaccines Drug Substance/Drug Product is manufactured and tested to cGMP requirements in the Grange Castle facility and to support the review and…

Their primary focus will be to enhance and maintain the quality oversight and compliance systems of validation activities on the Clonshaugh site.

You will support the specialist role function in each area. You will support new Validation and Commissioning programs across site as well as the periodic…

You will coordinate and execute all QA duties relating to QP batch release and communicate all issues. As part of the Pharmaceutical Diagnostics (PDx) business…

Reporting directly to the QA Manufacturing Supervisor. This role is necessary to provide quality compliance and quality technical support to Manufacturing…

Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.

Reporting to the Head of QARA Projects, you will provide QARA support for all on-going and new projects. Specifically, projects related to assay development and…

Support the development of the Design Development Plan in line with applicable regulations for combination products including Planning, Design and Development,…

Cpl with our client Pfizer is hiring for QA Stability Specialist on an initial 11-month contract for their site in Grange Castle, Dublin 22.

Cpl with our client Pfizer is looking for QA Specialist with validation experience to ensure that validation of the processes and lab equipment meets applicable…

This specific role is required to perform QA review of manufacturing and engineering records and associated documents and QA review and approval of procedures…

As a Quality Assurance Intern, you will collaborate closely with the QA team, where you will be responsible for various tasks, including testing software…