Team Lead QC Monitoring (m/w/d) — Lonza
Role overview
## Descrizione The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. In this leadership role, you will guide and develop a high‑performing monitoring team and ensure robust, compliant processes that support reliable manufacturing and patient safety. You will act as a key interface across functions while driving continuous improvement and operational excellence at site level.
## Cosa offriamo • An agile career path with opportunities to grow as a scientific and people leader. • An inclusive and ethical workplace that values collaboration and accountability. • Compensation programs that recognize leadership impact and performance. • A dynamic, cross‑functional role with strong site visibility and influence. • Ongoing development opportunities in leadership, GMP, and digital systems. • A supportive culture that encourages continuous improvement and innovation. • Competitive local benefits.
## Mansioni • You lead, coach, and develop a team of scientists and specialists to ensure high performance and engagement. • You allocate resources, prioritize workload, and ensure timely delivery of operational and project activities. • You conduct performance reviews, support career development, and foster an inclusive team culture. • You oversee daily monitoring operations, ensuring accurate data collection, review, and reporting. • You review complex data trends, investigations, and conclusions with scientific rigor and consistency. • You ensure GMP‑compliant documentation, including deviations, investigations, and preventive actions. • You collaborate closely with Operations, QA, Engineering, MSAT, and other stakeholders.
Description
## Descrizione The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. In this leadership role, you will guide and develop a high‑performing monitoring team and ensure robust, compliant processes that support reliable manufacturing and patient safety. You will act as a key interface across functions while driving continuous improvement and operational excellence at site level.
## Cosa offriamo • An agile career path with opportunities to grow as a scientific and people leader. • An inclusive and ethical workplace that values collaboration and accountability. • Compensation programs that recognize leadership impact and performance. • A dynamic, cross‑functional role with strong site visibility and influence. • Ongoing development opportunities in leadership, GMP, and digital systems. • A supportive culture that encourages continuous improvement and innovation. • Competitive local benefits.
## Mansioni • You lead, coach, and develop a team of scientists and specialists to ensure high performance and engagement. • You allocate resources, prioritize workload, and ensure timely delivery of operational and project activities. • You conduct performance reviews, support career development, and foster an inclusive team culture. • You oversee daily monitoring operations, ensuring accurate data collection, review, and reporting. • You review complex data trends, investigations, and conclusions with scientific rigor and consistency. • You ensure GMP‑compliant documentation, including deviations, investigations, and preventive actions. • You collaborate closely with Operations, QA, Engineering, MSAT, and other stakeholders.
