QC Laboratory Analyst (f/m/d)

The role of QC Laboratory Analyst (f/m/d) at Lonza involves working in a regulated environment to ensure product quality through various testing methods. Lonza is a company focused on manufacturing medicines, with a global presence across multiple continents. The company values diversity and fosters an inclusive environment for all employees. The main responsibilities include conducting and documenting physico-chemical analyses, ensuring compliance with regulatory standards, and managing laboratory equipment. This involves calibration, qualification, and maintaining associated documentation. The role also includes troubleshooting, investigating deviations, and implementing corrective actions. Additionally, the analyst will contribute to the development and optimization of laboratory processes and methods, support the training of new team members, and participate in on-call duties as scheduled. To qualify for this position, candidates must have a completed apprenticeship or degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific field. Several years of experience in Quality Control within a GMP-regulated environment is required, along with proficiency in physical and physico-chemical analytical techniques. These techniques include pH measurements, Karl Fischer titration, UV spectroscopy, osmolality, and conductivity measurements. A strong understanding of GMP and compliance requirements, as well as a structured and solution-oriented approach to work, is essential. The role requires good English skills and basic German proficiency. Nice-to-have skills include a collaborative mindset and a willingness to contribute to continuous improvement initiatives. The team at Lonza is known for its collaborative culture, built on openness, respect, and mutual support. The modern laboratory environment offers access to advanced technologies and analytical techniques, providing opportunities for professional and personal growth. What the role asks for: - Completed apprenticeship or degree in Chemistry, Biology, Pharmaceutical Sciences, or a comparable scientific discipline. - Several years of experience in Quality Control within a GMP-regulated pharmaceutical, biotech, or chemical manufacturing environment. - Experience with physical and physico-chemical analytical techniques, such as pH measurements. - Experience with physical and physico-chemical analytical techniques, such as Karl Fischer titration. - Experience with physical and physico-chemical analytical techniques, such as UV spectroscopy for protein concentration determination. - Experience with physical and physico-chemical analytical techniques, such as osmolality and conductivity measurements. - Good command of English. - Basic German skills.