This job is closed
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About the position
The QC Analyst position at Lonza involves supporting the Quality Control department in the production of drug lots for customers. This role includes conducting quality testing for ongoing customer stability studies and ensuring timely, high-quality results to meet manufacturing demands. The QC Analyst will apply their skills and company policies to complete various tasks, working on semi-routine assignments that require the ability to recognize deviations from accepted practices.
Responsibilities
- Running test samples for in-process, lot release and stability studies
- Reviewing assays
- Writing quality records (Deviations, CAPA, Change Control) and test methods
- Performing other duties as assigned
Requirements
- Bachelor's or associate Degree preferably in Microbiology, Biochemistry, or related science discipline
- 2-4 years industry experience preferably in a cGMP environment
- Use of Microsoft Suites (Word, Excel, PowerPoint)
- Use of Laboratory computer systems
- Experience using GMP Quality Systems such as: TrackWise, LIMS
