Equipment Validation Specialist, Level III

About the job

Lonza is a global leader in pharmaceutical manufacturing, dedicated to quality, innovation, and compliance. This role involves supporting GMP packaging, documentation, and process validation in a fully site-based environment, ensuring regulatory standards and operational excellence.

Requirements

• Bachelor’s degree in science or engineering
• GMP experience in pharma
• Knowledge of packaging validation
• Experience with technical documentation
• Strong problem-solving skills

Qualifications

• Detail-oriented and compliant mindset
• Effective communication skills
• Ability to manage multiple projects
• Team collaboration skills
• Commitment to quality and safety