- Location
- CH - Visp, Switzerland
- Type
- Full-time
- Source
- Workday
Description
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 dedicated individuals working together, brainstorming ideas that support businesses in making a positive impact on society. In return, we empower our employees to take ownership of their careers. Their innovative ideas, whether big or small, truly make a difference in the world. And that’s the type of work we aspire to contribute to.
Are you ready to take on the role of Data Reviewer (all genders) in our analytical Quality Control laboratory, located in the breathtaking Visp? Join our groundbreaking laboratory that boasts brand-new technology and instruments, and collaborate with a vibrant and international team. Your primary responsibilities will revolve around conducting routine analysis of biopharmaceuticals using HPLC and capillary electrophoresis techniques. In this role, you will also be responsible for reviewing data generated during routine Quality Control (QC) analysis in the QC Laboratory. Your expertise will ensure that all laboratory work aligns with GMP and SOPs, enabling the timely release of monoclonal antibody batches.
What you will get:
An agile scientific career in a dynamic, GMP‑regulated environment.
An inclusive and ethical workplace that values collaboration and accountability.
Compensation programs that recognize performance and technical expertise.
Opportunities to deepen your expertise and take ownership of impactful projects.
Exposure to cross‑functional collaboration and regulatory interactions.
A supportive culture that encourages continuous improvement and learning.
Competitive local benefits.
What you will do:
You review HPLC data and other laboratory-related raw data to ensure accuracy, completeness, and compliance.
You perform tasks within the gLIMS laboratory execution system, including creating consumable types and managing instruments and consumables.
You ensure all activities comply with GMP requirements and internal procedures.
You investigate ambiguous results with curiosity and attention to detail.
You adapt effectively to changing priorities in a dynamic Quality Control environment.
What we are looking for:
You have completed training as a laboratory technician or hold a bachelor’s degree in chemistry, biochemistry, or a related scientific field.
Experience in a GMP-regulated Quality Control environment is highly preferred.
Hands-on experience with HPLC and/or capillary electrophoresis (CE) is preferred.
You bring a highly detail-oriented, flexible, and investigative mindset.
You communicate fluently in English; German skills are a plus.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
