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The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. 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

  • Proactively maintain and continuously improve the production schedule.
  • Ensure departmental schedules are accurate and communicated to all relevant departments to drive short term execution of plans.
  • Create schedules respecting existing labor and asset capacities and based on planned material availabilities.
  • Drive timely resolution of all scheduling conflicts with relevant stakeholders.
  • Create, supervise and maintain short term schedules to provide awareness for defined departments.
  • Incorporate input from all relevant departments to ensure schedules are realistic within constraints and latest information.
  • Drive optimization of schedules by balancing demand priorities against optimal production sequencing and efficient resource utilization.
  • Ensure all feedback regarding changes to existing plans is incorporated into schedules in a timely manner.
  • Maintain detailed planning and scheduling parameters in planning system for optimal use of system scheduling functionality.
  • Generate relevant critical metric and operational measures to support identification of trends or root causes of sub-optimal performance.
  • Maintain accurate production schedule, providing data for the MRP process to meet production demands.
  • Review documents such as production schedules, work orders, and staffing tables to determine personnel and materials requirements, and material priorities.
  • Monitor production data, including volume produced, consumption of raw materials, and quality control measures, using this information for Continuous Improvement activities such as maintenance of routings and BOMs, increasing accuracy of production schedule and efficiency reporting.

Requirements

  • Bachelor’s Degree or equivalent experience with extensive years of proven experience in end-to-end Supply Chain.
  • Solid knowledge in APICS CPIM professional standards is an advantage.
  • Strong SAP background with skills in financial, scheduling and materials planning is a must.
  • Planview background is an additional benefit.
  • Demonstrates the courage and integrity to engage in difficult conversations with internal teams and management when needed, encouraging transparency, growth, and collaboration.
  • Strong communication and presentation skills, ability to present ideas in a clear and concise manner.
  • Change adaptability skills.
  • Proficient in English and German (spoken and written).

Benefits

  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.
  • A variety of benefits dependent on role and location.
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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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