Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

Join Lonza in Visp as a QA Manager Deviations (m/f/d) and become an integral part of a talented team dedicated to making a global impact in the field of life sciences. This position based in Switzerland is essential in maintaining compliance with regulatory requirements and internal quality standards. You will have the opportunity to contribute directly to the continuous improvement of our world-class quality management system in a collaborative and ambitious environment.

Key responsibilities:

• Review and approve deviation reports to ensure completeness, accuracy, and compliance with regulatory requirements (e.g., FDA, EMA) and internal quality standards.
• Evaluate proposed root cause analyses and CAPA to ensure adequacy in preventing recurrence.
• Collaborate with multi-functional teams (e.g., manufacturing, QC, engineering) to ensure quality issues are addressed and resolved appropriately.
• Supervise deviation trends and quality metrics to identify areas for improvement and report findings to senior management.
• Drive continuous improvement initiatives related to deviation management processes.
• Support internal and external audits, inspections, and regulatory submissions by providing information on deviation management practices.
• Provide mentorship and training to staff on deviation management and related quality topics.

Key requirements:

• Bachelor degree or equivalent experience in Life Sciences, Pharmacy, Biotechnology, or a related field.
• Sufficient experience in Quality Assurance within the pharmaceutical or biotech industry, with a focus on deviation management.
• Strong knowledge of regulatory requirements (e.g., FDA, EMA, ICH) related to quality management.
• Experience with quality management systems (e.g., TrackWise, Veeva) and CAPA processes.
• Excellent attention to detail and problem-solving skills.
• Strong communication and interpersonal skills, with the ability to work collaboratively in a cross-functional environment.
• Proficient English is required and good German language skills – an advantage.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.