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Materials Specialist

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Onsite

Materials Specialist

Independent Solutions

Materials Specialist

Skills

Testing & QARSAP ERPSupply ChainComplianceRegulatory Compliance

2 days ago

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Important information


Contract type:

Freelance / Contract

Location:

Dunboyne, Co. Meath, Ireland

Work mode:

Onsite

Published on:

22 October 2026

What they need


Job Title- Material Specialist- Pharmaceutical

Location: Dunboyne, Co. Meath

Work Arrangement: Hybrid – 3 days onsite per week

Job Overview

We are seeking an NMI & MQ Specialist to manage the introduction, qualification and lifecycle management of materials used in a pharmaceutical manufacturing environment. The successful candidate will ensure that new and existing materials meet quality, regulatory and safety requirements while supporting compliant, reliable and cost-effective supply.

Key Responsibilities

  • Manage change controls and resolve gaps arising from supplier change notifications.
  • Lead end-to-end New Material Introduction (NMI) activities, including technical evaluations and supplier qualification.
  • Plan, coordinate and execute material qualification activities to ensure compliance with regulatory standards, safety requirements and product specifications.
  • Prepare, review and maintain technical documentation required for material approval.
  • Coordinate the introduction of new materials to meet site requirements, quality standards and project timelines.
  • Collaborate with suppliers, procurement, R&D, process engineering, Quality Assurance, regulatory teams and manufacturing operations.
  • Support material qualification processes, regulatory compliance and internal and external audits.
  • Maintain and update approved material lists and qualified material databases.
  • Lead root-cause investigations and corrective and preventive actions for recurring material issues.
  • Drive continuous improvement initiatives to enhance NMI and Material Qualification (MQ) processes.
  • Build and maintain effective relationships with suppliers and internal stakeholders.

Essential Requirements

  • A university degree in Engineering, Pharmacy, Science or a related discipline.
  • Minimum 4 years of relevant experience in a technical, supply chain, documentation or material-related role.
  • Experience working with technical documentation and document management.
  • Pharmaceutical industry experience is preferred and may be required depending on the candidate's background.
  • Strong communication, collaboration and stakeholder management skills.
  • Excellent organisational skills, initiative and the ability to manage multiple priorities.
  • Proficiency in Microsoft Office, particularly Excel.

Preferred Experience

  • Experience in New Material Introduction, Material Qualification or new product introduction within the pharmaceutical industry.
  • Knowledge of SAP, particularly master data and production execution modules.
  • Understanding of single-use materials and relevant qualification standards.
  • Experience managing supplier change notifications, material-related investigations and supplier issues.
  • Familiarity with change controls, root-cause analysis and continuous improvement initiatives.
  • Ability to develop process-based solutions and work effectively across cross-functional teams.

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