Group Leader, Drug Linker-Toxin Development

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career culture

Inclusive workplace

Competitive compensation

Zusammenfassung

Lonza in Visp, Switzerland, is seeking a Group Leader Development / MSAT for Drug Linker-Toxin to guide chemists, drive technology transfer, and maintain GMP manufacturing readiness. This is a hands-on leadership role combining scientific depth with people management in an ADC setting.

You will align closely with production facilities, shape the roadmap for capability and capacity, mentor scientists, ensure safety and containment compliance, and contribute to external scientific content and

Qualifikationen

• PhD in Chemistry, Chemical Engineering, or a related discipline; PhD in Organic Chemistry preferred.
• Approximately 5–10 years of experience in pharmaceutical process development, API development, clinical supply, or manufacturing sciences.
• Proven experience leading complex projects in a matrix organization within clinical supply, development, or manufacturing operations.

Aufgaben

• Lead, coordinate, execute, control, and monitor the performance of assigned Drug Linker-Toxin Process Development and/or MSAT chemists in line with objectives.
• Support the Head in managing and allocating required chemist resources.
• Guide chemists to enable efficient transfer of production processes into GMP facilities.
• Drive development and implementation of technologies to increase capability, capacity, and efficiency.

Kenntnisse

Leadership

GMP knowledge

Containment expertise

English fluency

German knowledge

Ausbildung

PhD in Chemistry or related discipline

Tools

GMP manufacturing tools

Containment equipment experience

Jobbeschreibung

Lonza in Visp, Switzerland, is seeking a Group Leader Development / MSAT for Drug Linker-Toxin to guide chemists, drive technology transfer, and maintain GMP manufacturing readiness. This is a hands-on leadership role combining scientific depth with people management in an ADC setting.

You will align closely with production facilities, shape the roadmap for capability and capacity, mentor scientists, ensure safety and containment compliance, and contribute to external scientific content and