Pharma Materials Specialist – NMI & MQ Expert

Independent Solutions; Dunboyne; Híbrido; EUR 60.000 - 75.000; Jornada completa

Descripción de la vacante

Independent Solutions is seeking a Material Specialist- Pharmaceutical in Ireland. The role focuses on managing NMI and MQ activities, supplier qualification and lifecycle management of materials used in pharmaceutical manufacturing.

You will lead change controls, qualification plans and document preparation, collaborating with procurement, R&D, QA, regulatory, and manufacturing teams to ensure compliant, cost-effective supply and reliable material performance.

Formación

• University degree in Engineering, Pharmacy, Science or related discipline.
• Minimum 4 years of relevant experience in a technical, supply chain, documentation or material-related role.
• Experience with technical documentation and document management.
• Pharmaceutical industry experience preferred.

Responsabilidades

• Lead end-to-end New Material Introduction and supplier qualification activities.
• Manage change controls and address supplier change notifications.
• Plan and execute material qualification to ensure regulatory and safety compliance.
• Prepare technical documentation for material approvals.
• Coordinate introduction of new materials to meet site requirements and timelines.
• Collaborate with suppliers, procurement, R&D, process engineering, QA and manufacturing.
• Support audits and maintain approved material lists and databases.
• Lead root-cause investigations and CAPA for material issues.

Conocimientos

Change controls

Supplier qualification

Project coordination

Communication skills

Excel, MS Office

Educación

Bachelor's degree in Engineering, Pharmacy, Science

Herramientas

SAP

Document management

Descripción del empleo

Independent Solutions is seeking a Material Specialist- Pharmaceutical in Ireland. The role focuses on managing NMI and MQ activities, supplier qualification and lifecycle management of materials used in pharmaceutical manufacturing.

You will lead change controls, qualification plans and document preparation, collaborating with procurement, R&D, QA, regulatory, and manufacturing teams to ensure compliant, cost-effective supply and reliable material performance.