Alle Stellen

Drive supply chain excellence and quality compliance at our high-impact Visp site by leading critical project initiatives that ensure our material management processes are inspection-ready and robust. In this high-visibility project management role, you will bridge logistics, quality assurance, master data, and IT to directly enhance production reliability for life-saving medicines. This is a fully site-based role, supporting close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

Start date: As soon as possible

Contract Duration: Until 31 Dec 2026

Location: Visp, Switzerland

Hours: 41 hours per week

Tasks

  • Lead and coordinate cross-functional quality improvement projects and remediation workstreams impacting Supply Chain Operations.
  • Translate compliance and audit findings into structured project plans, milestones, deliverables and risk mitigation strategies.
  • Leverage SAP (Material Master) expertise to analyze process gaps, data quality issues and master data ownership models.
  • Build alignment and drive execution across Supply Chain, Quality Assurance, Manufacturing, MSAT, Master Data and IT functions.
  • Support the definition and documentation of sustainable material management controls and standardized governance routines.
  • Maintain project governance, meeting cadences, progress tracking and management reporting for remediation activities.
  • Ensure all project documentation, data reconciliation, and evidence are structured, compliant and inspection-ready.

Requirements

  • Bachelor’s or Master’s degree in Supply Chain, Business Administration, Engineering, Life Sciences, Information Systems or a related field.
  • Senior project management experience driving quality remediation, compliance, or material management projects in a highly regulated GMP environment (Pharma, Biotech, or CDMO).
  • Proven ability to orchestrate cross-functional stakeholders across Supply Chain, Quality Assurance, MSAT and shop-floor manufacturing operations.
  • Strong data management and analytical skills; proficiency with data tools such as Excel and Power BI is preferred and highly valued.
  • Solid background in SAP Material Master, material classification, and supplier data collection (SDS / technical specifications), combined with hands-on experience in CAPA-like action tracking, quality systems, and audit readiness standards.
  • Excellent cross-functional stakeholder management, facilitation and escalation skills.
  • Business fluency in English is required along with working proficiency in German.

Benefits

  • An agile career and dynamic working culture.
  • An inclusive and ethical workplace.
  • Competitive hourly rate.
  • Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.
Bist du Teil dieses Unternehmens?

Dieses Unternehmensprofil wurde automatisch erstellt. Wenn du für Lonza Group AG arbeitest, kannst du das Profil jetzt beanspruchen und verifizieren – kostenlos und in wenigen Minuten.

Verifizierte Profile erhalten ein Siegel und können ihre Seite, Stellen und Bewerbungen direkt verwalten.
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.
Ähnliche Stellen