Senior QC Analyst
About The Position
The Quality Control (QC) Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza's manufacturing demands. A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Requirements
- Bachelor's or Associate's Degree preferably in Microbiology, Biochemistry, or related science discipline.
- Use of Microsoft Suites (Word, Excel, PowerPoint).
- Use of Laboratory computer systems.
- Experience using GMP Quality Systems such as: TrackWise, LIMS preferred.
Responsibilities
- Running test samples for in-process, lot release and stability studies.
- Reviewing assays.
- Writing quality records (Deviations, CAPA, Change Control) and test methods.
- Performs other duties as assigned.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Professional, Scientific, and Technical Services
Number of Employees
5,001-10,000 employees
