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Chromatography Principal Scientist

Sanofi
Full-time
Remote friendly (Cambridge, MA)
United States
$122,250 - $176,583.33 USD yearly
Clinical Research and Development

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Role Summary

Chromatography Principal Scientist responsible for analytical support to chemistry teams and development of analytical methods for small molecules using HPLC, UHPLC, GC, and potentiometry.

Responsibilities

  • Develop specific and robust analytical methods using equipment including HPLC, UHPLC, GC, and be responsible for validating the methods when necessary
  • Analyze synthetic molecules mainly by HPLC/UHPLC, GC, potentiometry, and TLC
  • Perform quantification of impurities
  • Perform mass balance studies
  • Design and implement analytical strategies for synthesis intermediates and raw materials
  • Develop effective collaborations with others within project teams and between analytical groups
  • Generate technical reports independently
  • Share knowledge and experience of analytical method development for synthetic molecules
  • Introduce innovative analytical approaches to facilitate optimal decision-making
  • May serve as a project lead

Qualifications

  • A Master’s degree or equivalent in Analytical Chemistry or related field with a minimum of 8 years, or a PhD with minimum of 5 years of experience in the pharmaceutical/biotech industry. A PhD in Analytical Chemistry is preferred.
  • Expertise in the operation of LC and GC
  • Familiarity with the operation of potentiometry titrator, and TLC from multiple manufacturers
  • Extensive experience in method development using HPLC/UPLC and GC
  • Experience in analytical method validation
  • Record of adhering to and promoting lab safety practices
  • Good communications skills

Preferred Qualifications

  • In-depth understanding of the separation principles of LC, GC and method development software
  • Deep expertise in chromatography method development and trouble shoots
  • Knowledge of QbD concepts, specification setting, and cGMP, with experience in contributing to regulatory submission
  • Communicates effectively in individual and group settings and collaborate effectively in a multi-disciplinary team setting
  • Demonstrated project management skills
  • Consistent record of collaboration with scientists and other stakeholders at external enterprises
  • Advanced scientific network in the industry and academia
  • Record of patents and publications
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