New Material Introduction

OverviewJob DescriptionA fantastic opportunity has arisen for a New Material Introduction & Material Qualification Specialist at our new state of the art single use multi-product biotech facility in Dunboyne, County Meath, Ireland.ResponsibilitiesLead end-to-end new material introduction (NMI) activities, from technical evaluation and supplier qualification.Plan, coordinate and execute material qualification to ensure new materials comply with industry regulations, safety standards and product specific requirements.Generate and review technical documentation required for material approval.Ensure new materials are introduced on site to enable successful release to meet schedule needs while prioritising safety and quality.Serve as the primary interface for material suppliers, procurement, R&D, process engineering, QA, regulatory and operations for NMI projects.Responsible for materials introduction and qualification process.Work with partners to manage these activities and refine the processes in alignment with regulatory and company procedures and support regulatory and company compliance audits.Maintain and update the approved materials list, qualified materials database.Drive root-cause corrective actions and preventive measures for recurring material issues; lead cross-functional continuous improvement projects.Continuously improve the NMI & MQ process on site.Build an excellent relationship with suppliers assigned to ensure value is created and delivered for the site.Required SkillsBachelor's degree in engineering, pharmacy or science related field.Minimum four (4) years previous experience within a Supply Chain or technical role associated with new product introduction in a pharmaceutical environment.Sense of initiative and urgency, ability to work with multiple stakeholders to develop process-based solutions and manage the associated communications effectively.SAP systems knowledge – master data, production execution modules.Ideally, experience of single-use materials and applicable regulatory standards for the qualification of single use materials.Previous experience with engagement with vendors on material related issues including supply chain notifications and investigations.Effective communicator to manage both internal and external stakeholders that support the site.Collaboration skills and teamwork mindset.Enterprise mindset to ensure the right priorities are set for the site.Computer literate with advanced skills in MS Office, especially Excel.Ability and willingness for continuous learning.Ability to challenge the status quo with a continuous improvement mindset.Preferred SkillsCurrent Employees apply HERECurrent Contingent Workers apply HEREOther Job RequirementsThis role is a hybrid role; onsite support will be required based on day-to-day activities.As a company, we are committed to keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world\'s most challenging healthcare needs.As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together.Please don\'t hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.We are committed to flexible working where possible, and this is why our Company has introduced a new hybrid working model for office-based colleagues around the world.Please feel free to speak to us about what flexibility means to you during your application.Next StepsSo, if you are ready to: Invent solutions to meet unmet healthcare needs, please apply today.Job DetailsJob Posting End Date: 10/29/2025Requisition ID: R******#J-*****-Ljbffr