Supply Chain Quality Project Manager

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career culture

Inclusive workplace

Competitive hourly rate

Zusammenfassung

Lonza Visp site in Switzerland seeks a Senior Project Manager to drive supply chain excellence and quality compliance in life sciences manufacturing. You will bridge logistics, quality assurance, master data and IT to improve production reliability for medicines.

This is a fully site-based role with a 41-hour workweek, requiring close collaboration in person. You will coordinate remediation workstreams, translate audit findings into plans, and maintain governance and inspection-ready

Qualifikationen

• Senior project management experience driving quality remediation in GMP environments (Pharma/Biotech/CDMO).
• Proven ability to orchestrate cross‑functional stakeholders across Supply Chain, Quality Assurance, MSAT and shop-floor operations.
• Strong data management and analytical skills; Excel/Power BI familiarity is valued.
• Fluent English and working German language skills are required.

Aufgaben

• 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.

Kenntnisse

Project management

Cross-functional leadership

Data analysis

Excel

Power BI

Stakeholder management

English (business)

German (working)

Ausbildung

Bachelor's or Master's in Supply Chain/Engineering/Life Sciences/IS

Tools

SAP Material Master

CAPA tracking

Jobbeschreibung

Drive supply chain excellence and quality compliance at our high-impact Visp site, 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. Working together in person supports 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

Hours: 41 hours per week

What you will get:

• 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.

What you will do:

• 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.

What we are looking for:

• 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.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment.