The incumbent for this position will be responsible for the development and validation of analytical methodologies and performance of tasks using chromatographic, spectroscopic, solid-state, and physical/wet-chemical techniques.
Develop, validate, and transfer analytical methods
Work with various analytical methods including cleaning verification, assay and related substances, dissolution, residual solvents in-process control, and analysis of finished products and excipients
Review/analyze data and information for technical correctness and accuracy; interpret and evaluate results properly
Perform initial and stability testing for R&D batches and demonstration batches to support formulation development
Perform laboratory instrumentation qualification, preventative maintenance, calibration, and minor repair with proper documentation
Bachelor’s degree in chemistry, pharmaceutical sciences, or related field required; Master's or PhD preferred
3+ years’ experience in pharmaceutical analytical development or quality control
Familiarity with chromatographic (HPLC/GC), spectroscopic, and solid-state characterization techniques preferred
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