Full-time Posted June 04, 2026
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Job Description

Job Description

  • Perform stability testing on pharmaceutical products according to approved protocols and timelines.
  • Execute chromatographic analyses including HPLC/LCUPLC‑UV, and GC following validated methods.
  • Conduct sample preparation (dilutions, extractions, filtrations, weighing, etc.) with strong attention to accuracy and traceability.
  • Ensure all testing is performed in compliance with GMPSOPs, and regulatory requirements.
  • Assist in method development and optimization, including evaluating chromatographic conditions, sample prep techniques, and detection parameters.
  • Record all activities in laboratory notebooks or electronic systems in accordance with ALCOA+ data integrity principles.
  • Review and interpret analytical data, ensuring accuracy before reporting results.
  • Operate, calibrate, and maintain analytical instruments (HPLC/UP...
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