QC Associate, Analyst
lonza.com
- Required language
- German conversational, English conversational
- Job written in
- English
- Location
- Visp
- Work type
- On-site
- Type
- Full-time
The QC Associate, Analyst role at Lonza involves working in a demanding GMP-regulated setting, focusing on physical and physico-chemical analyses to ensure product quality. The company specializes in manufacturing medicines and therapies, with a strong emphasis on innovation and collaboration. The main responsibilities include conducting, evaluating, and documenting physico-chemical analyses according to cGMP standards and regulatory guidelines. This role also involves managing laboratory equipment, troubleshooting issues, and implementing corrective actions. Additionally, the analyst will support the development and optimization of laboratory processes and assist in training new team members. Participation in the on-call duty rota is also required. To qualify, candidates must have completed an apprenticeship or degree in Chemistry, Biology, Pharmaceutical Sciences, or a related scientific field. Experience in Quality Control, particularly in a GMP-regulated environment, is essential. Specific analytical techniques such as pH measurements, Karl Fischer titration, and UV spectroscopy for protein concentration determination are required. A strong understanding of GMP and compliance requirements is also necessary. Nice-to-have skills include a collaborative mindset and a willingness to contribute to continuous improvement initiatives. The role is based in Visp, Switzerland, and relocation assistance is available for eligible candidates and their families. The team at Lonza values diversity and fosters an inclusive environment, encouraging collaboration and mutual support. What the role asks for: - Completed apprenticeship or degree in Chemistry, Biology, Pharmaceutical Sciences, or a comparable scientific discipline. - Initial or several years of experience in Quality Control, ideally 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. - Strong quality mindset and understanding of GMP and compliance requirements. - Good command of English and basic German skills.
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