Senior GMP Deviation Investigator & CAPA Lead

Lonza Group Ltd.; Oberwallis; On-site; CHF 120,000 - 170,000; Full time

Benefits offered by this job

Agile career culture

Inclusive workplace

Competitive compensation

Benefits depend on role and location

Job summary

Lonza Visp, Switzerland, seeks a Senior Deviation Specialist to lead complex GMP deviation investigations and drive CAPAs across functions. You will collaborate with Manufacturing, Quality Control, and Engineering to gather data, interpret findings, and ensure compliant reports in line with global regulatory expectations.

This site-based role emphasizes real-time collaboration and rigorous quality standards to maintain product safety and process reliability across the manufacturing network.

Qualifications

• Experience in GMP-regulated pharma/biotech quality systems.
• Experience with deviation management and CAPAs.
• Knowledge of cGMP and regulatory expectations (FDA/EMA/ICH).

Responsibilities

• Lead GMP deviation investigations and drive CAPAs.
• Author compliant deviation reports and support audits.
• Monitor CAPA effectiveness and prevent recurrence.
• Collaborate with Manufacturing, Quality Control, and Engineering.

Skills

Root cause analysis

GMP deviations

Cross-functional collaboration

Data interpretation

German & English

Education

Science or Engineering degree

Tools

TrackWise

Veeva

Job description

Lonza Visp, Switzerland, seeks a Senior Deviation Specialist to lead complex GMP deviation investigations and drive CAPAs across functions. You will collaborate with Manufacturing, Quality Control, and Engineering to gather data, interpret findings, and ensure compliant reports in line with global regulatory expectations.

This site-based role emphasizes real-time collaboration and rigorous quality standards to maintain product safety and process reliability across the manufacturing network.