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The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Lead and inspire a QA Material Management & Supply Chain team, ensuring GMP compliance, supplier quality, and seamless material lifecycle management from sourcing to release. Bring your leadership expertise and strong stakeholder management skills to drive quality excellence, continuous improvement, and cross-functional collaboration in a dynamic pharmaceutical environment. This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

Tasks

  • Lead, develop, and manage the QA Material Management & Supply Chain team across different seniority levels, ensuring performance, capability, and compliance.
  • Ensure GMP compliance across the full lifecycle of raw materials and primary packaging materials from sourcing to release.
  • Ensure QA oversight for raw material release and warehousing practices.
  • Ensure QA governance of warehouse and logistics processes, including goods receipt, material flow, and master data integrity.
  • Oversee supplier quality management, including supplier qualification, quality agreements, performance monitoring, and supply chain integrity.
  • Oversee introduction and lifecycle management of new materials and suppliers, ensuring GMP compliance and cross-functional alignment.
  • Review and approve critical QA documentation, including specifications, SOPs, validation documents, deviations, and changes, where applicable.
  • Act as escalation point and decision authority for complex quality issues related to materials, suppliers, and supply chain.
  • Support audits and inspections, ensuring readiness across local supplier management, material processes, and logistics.
  • Drive continuous improvement, KPI management, and cross-functional collaboration across QA, QC, Supply Chain, and Manufacturing.

Requirements

  • You are an experienced people leader and you emphasize listening to and coaching your team.
  • You have proven experience in building strong relationships – also with difficult stakeholders or stakeholder groups.
  • Extensive experience in QA in pharmaceutical GMP environment with focus on material management as well as supply chain (warehousing and supplier quality management).
  • Academic degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or related field.
  • Fluency in English is a must.
  • Fluency in German is a plus.

Benefits

  • An agile career and a dynamic work culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits.
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Über uns
Lonza Group AG ist ein international tätiges Unternehmen für die Pharma-, Biotech- und Life-Science-Industrie. Das Unternehmen entwickelt und produziert Wirkstoffe, biopharmazeutische Produkte sowie spezialisierte Lösungen und unterstützt Kunden von der frühen Entwicklung bis zur industriellen Herstellung. Zudem stellt Lonza chemische und biotechnologische Komponenten für Anwendungen in Gesundheit, Ernährung und weiteren Industrien her.
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