Team Lead QC Monitoring (m/w/d)

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.

What you will get:

• 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.

Benefits in Visp:
https://bit.ly/3wjkoFi

What you will do:

• 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.

What we are looking for:

• You hold a university degree in life sciences or a related scientific field.

• You bring 3–5 years of experience in a GMP‑regulated environment.

• You have experience leading, mentoring, or coordinating scientific or technical teams.

• You possess a strong understanding of regulatory standards, including EU GMP Annex 1 and pharmacopoeias.

• You are experienced with digital systems such as MODA, LIMS, or DMS.

• You communicate confidently in both English and German.

• You work in a structured, accountable, and solution‑oriented manner.

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 for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.