Senior Specialist Supplier Quality - Permanent

  • Dublin
  • Alexion Pharmaceuticals
This is what you will do:Within the Supplier Quality team, you’ll become part of a team of professionals working with all aspects of the Alexion business from development to commercialization and distribution. You will support the management of the Supplier Quality program for all of Alexion. Assist in the Supplier and Material approval process and in the management of all Supplier Quality inputs including quality agreements, questionnaires, audits, supplier corrective action reports, supplier change notifications, Alexion change control, etc. Assist in the preparation of inputs to the Supplier Management Review process, including preparation of data for the review. Assist in the monitoring and reporting of supplier performance indicators and contribute to the quality improvement opportunities within the supply chain.You will be responsible for:Support the global supplier qualification and oversight processes including migration to Enterprise systems..Support Supplier Change Notification process to ensure appropriate change control and regulatory updates have been made prior to making changes.Perform monitoring of approved Suppliers through data gathering and reporting.Perform periodic review of approved Suppliers.Gather data and report quality metrics for internal processes and identify and implement improvement opportunities.Lead Continuous Improvement projects for Supplier Quality SystemDevelop and deliver SQ Process TrainingAct as Supplier Quality SME for audits and inspections.Perform all responsibilities in accordance with company policies, procedures, federal regulations and safety requirements.You will need to have:Minimum of 6+ years’ experience working in a GMP environment with experience in Supplier Qualification and Oversight including authoring Quality Agreements.Experience with Quality Risk Management and Structured Problem-Solving toolsA strong customer focus and ability to prioritize and adapt to business needsKnowledge of applicable international GXP regulations and standardsStrong business partner with a focus on delivering results.Excellent written and verbal communication skillsStrong ability to analyse systems and dataCapable of identifying and mitigating risksExperience with high performance teams, cross functional projects.We would prefer for you to have:Experience with Technical WritingExperience working with mature supplier quality systemPrevious global Quality System development/deployment experienceExperience supporting regulatory inspectionsDate Posted26-Mar-2024Closing Date29-Apr-2024Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.