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Lannett Company

Analytical Services Chemist II

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Summary

This position is primarily responsible for the laboratory testing of raw materials, packaging materials, in-process, release and stability samples for pre-commercial drug products, including the evaluation of new raw materials, new packaging materials, reference standard qualifications, method transfers, and method validations within the framework of cGMP compliance guidelines.

Responsibilities

  • Perform routine and non-routine physical and chemical tests and assays on raw materials, API’s, in-process, finished products, experimental batches and associated stability studies
  • Testing performed to include basic and complex lab equipment and procedures, such as pH, Loss on Drying, Residue on Ignition, Water Content by Karl Fischer, Assay/Impurities by HPLC, Dissolution, Residual Solvents by GC, and wet chemistry techniques such as titrations and sample derivatizations
  • Execute method transfer/validation protocols for basic analytical test methods for drug substance/product assay/dissolution/ residual solvents according to ICH/FDA/USP requirements under minimal supervision
  • Draft method transfer/validation reports for basic analytical test methods for drug substance/product assay/dissolution according to ICH/FDA/USP requirements under minimal supervision
  • Develop and validate analytical Cleaning Validation methods and perform testing of cleaning validation samples and generate analytical report with supervision.
  • Document all laboratory testing and maintain accurate and legible notebooks and records
  • Provide regular update progress reports of projects
  • Comply with all relevant regulatory requirements
  • At all times strive to maintain the self-esteem of individual team members and the professionalism of the group as a whole
  • Perform laboratory troubleshooting, propose solutions and implement
  • Other projects and duties as required or assigned

Experience

  • BS Degree in Chemistry or related field and 2 - 4 years of pharmaceutical product analysis experience in a cGMP-regulated lab environment
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