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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. In this role, you will contribute to robust monitoring activities by evaluating complex data, improving processes, and supporting compliance in a GMP‑regulated environment. You will work closely with cross‑functional partners and play an active role in inspections and continuous improvement initiatives.
Tasks
- You collect, evaluate, and summarize monitoring data using MODA, LIMS, and digital analysis tools.
- You document GMP‑relevant activities and lead investigations of alert or action level excursions.
- You drive root‑cause investigations and align corrective actions with key stakeholders.
- You create, review, and approve DMS documents to ensure accuracy and compliance.
- You improve monitoring processes to enhance data quality, efficiency, and robustness.
- You implement monitoring updates and manage MODA‑related changes under change control.
- You represent the team during inspections, audits, and customer visits with confidence.
Requirements
- You hold a degree in life sciences or a related scientific field.
- You bring around two years of relevant experience in a GMP‑regulated environment.
- Experience in environmental monitoring and/or microbiology is an advantage.
- You have strong digital skills, including Microsoft Office and documentation systems.
- Knowledge of regulatory requirements, pharmacopoeias, and EU Annex 1 is ideal but not required.
- You communicate confidently in English; German skills are a plus.
- You work independently and bring a proactive, detail‑oriented, solution‑focused mindset.
Benefits
- An agile scientific career in a dynamic, GMP‑regulated environment.
- An inclusive and ethical workplace that values collaboration and accountability.
- Compensation programs that recognize performance and technical expertise.
- Opportunities to deepen your expertise and take ownership of impactful projects.
- Exposure to cross‑functional collaboration and regulatory interactions.
- A supportive culture that encourages continuous improvement and learning.
- Competitive local 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.