Material Life Cycle Management Specialist

Pauwels Consulting; Geel; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

Pauwels Consulting is assisting a leading pharmaceutical organization in Antwerp to strengthen its material life cycle management team on a temporary basis. The role blends technical and organizational tasks within a modern production environment.

You will manage onboarding and maintenance of materials, align procedures to standards, and drive continuous improvement using Excel, Power BI, and PowerPoint. The position emphasizes data-driven decision making and proactive collaboration with

Qualifications

• Experience working in a GMP pharmaceutical production facility.
• Advanced skills in Excel, Power BI, and PowerPoint.
• Strong data-driven mindset and ability to assess material criticality from data.
• Proactive, curious, and solution-oriented in a dynamic environment.
• Excellent communication and stakeholder engagement.

Responsabilités

• Onboard and maintain materials/services, including supplier change compliance.
• Align local procedures with standards; close gaps via change control.
• Identify/qualify alternative suppliers to prevent production delays.
• Migrate docs into updated templates for evolving workflows.
• Identify cost-reduction opportunities for direct/indirect items.
• Optimize data systems with Excel and Power BI for CI goals.
• Support projects across R&D, MSAT, and QC teams.

Connaissances

GMP experience

Data analysis

Communication

Outils

Excel

Power BI

PowerPoint

Description du poste

Our client, a leading pharmaceutical organization, is seeking an energetic professional to temporarily strengthen their material life cycle management team. This role offers a diverse mix of technical and organizational challenges within a modern production environment.

• Manage the onboarding and maintenance of new materials and services, including compliance checks for supplier changes.
• Research and align local procedures with internal and external standards, addressing gaps through change control processes.
• Ensure business continuity by identifying and qualifying alternative supply options to prevent production delays.
• Migrate technical documentation into updated templates to support evolving operational workflows.
• Identify cost-reduction opportunities for direct and indirect items while maintaining high quality standards.
• Optimize data systems and processes using Excel and Power BI to support continuous improvement goals.
• Provide support for technical projects involving R&D, MSAT, and QC departments.

• You bring experience working within a GMP environment at a pharmaceutical production facility.
• You possess advanced proficiency in digital tools, specifically Excel, Power BI, and PowerPoint.
• You have a strong affinity for technical processes and the ability to assess the criticality of materials and services based on data.
• You're proactive, curious, and maintain a solution-oriented mindset in a dynamic work environment.
• You possess excellent communication skills and the confidence to challenge the status quo and engage with stakeholders.

Nice to Haves

• Experience with specific QC, MSAT, or R&D interfaces.
• Familiarity with continuous improvement methodologies and OPEX principles.