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Quality Control (LC-MS)

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Onsite

Quality Control (LC-MS)

Marksans Pharma

Quality Control (LC-MS)

2 months ago

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Important information


Contract type:

Permanent

Work mode:

Onsite

Published on:

10 August 2026

What they need


  • Operate, maintain, and troubleshoot LC-MS/LC**-**MS/MS instruments and associated software.
  • Perform routine and non-routine analysis of finished products, intermediates, raw materials, impurities, degradation products, and stability samples.
  • Execute approved analytical methods and laboratory procedures in accordance with SOPs and specifications.
  • Perform sample preparation, dilution, filtration, extraction, and other required analytical procedures.
  • Develop a basic understanding of mass spectrometry principles, including ionization, mass selection, fragmentation, and detection.
  • Perform qualitative identification and quantitative estimation using LC-MS/LC-MS/MS.
  • Optimize and monitor LC-MS/MS parameters such as source conditions, MRM/SRM transitions, collision energy, gas flow, and chromatographic conditions.
  • Review chromatograms, mass spectra, system suitability results, and analytical data.
  • Perform instrument qualification, calibration, preventive maintenance, and routine performance checks in coordination with engineering/service teams.

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