Barden are delighted to be supporting our Global Pharmaceutical client in their search for Quality Specialist for their state-of-the-art facility in Dublin.
ABOUT THE ROLE:
This is an initial 9-month contract, on a hybrid basis of 3 days onsite and 2 days remote. You will report into the Director of Supplier Quality and will be primarily responsible for assisting in the management of the global suppliers and materials qualification.
RESPONSIBILITIES:
* Assist in managing the global supplier and material approval processes, including transitioning site-specific procedures to the global framework.
* Provide support in overseeing the Quality Agreement management process.
* Facilitate the Supplier Change Notification process, ensuring that proper change control measures and regulatory updates are implemented before changes are executed.
* Contribute to the preparation of materials for Supplier Reviews, including compiling review data, summarizing outcomes, and tracking supplier-related complaints to foster improvements.
* Support the monitoring and reporting of supplier performance metrics, while identifying opportunities for quality enhancements within the supply chain.
* Contribute to the continuous improvement of the Supplier Quality Management System.
ABOUT THE PERSON:
* Minimum of a B.Sc. degree in Science / Engineering discipline.
* Minimum of 2+ years’ experience in a GMP facility.
* Familiarity with SAP and Veeva EQV would be desirable.
* An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing and Biotechnology Research
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