Join Lonza as a QA Specialist I, Compliance, where you will support document control and quality systems to ensure compliant GMP operations. This is an exciting opportunity to contribute to quality excellence and patient impact.
Requirements
- Experience in a regulated environment, preferably pharmaceuticals
- Basic knowledge of GMP and FDA regulations
- Familiarity with QMS tools, or willingness to learn
- Strong written and verbal communication skills
- High attention to detail and organizational skills
- Ability to manage multiple tasks and deadlines
Benefits
- An agile career and dynamic working culture
- An inclusive and ethical workplace
- Compensation programs that recognize high performance
- Medical, dental, and vision insurance
- Opportunities for learning and career growth
- A collaborative and supportive team environment
- Access to global Lonza benefits programs