About the Role
Job description
As Quality Control Analytical Chemist, you will perform routine QC release and stability testing for pharmaceutical products under cGMP. Core work includes preparing samples and standards, executing HPLC and GC analyses, documenting results to data integrity (ALCOA+) standards, and supporting investigations as needed. You’ll collaborate with QC, Stability, and Documentation teams to ensure timely testing, compliant records, and right-first-time execution.
Key responsibilities
- Execute compendial and validated methods for HPLC and GC (system suitability, injec...
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