Chromatography Principal Scientist at Sanofi
Cambridge, MA 02139, USA -
Full Time


Start Date

Immediate

Expiry Date

29 Nov, 25

Salary

176583.33

Posted On

29 Aug, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Analytical Chemistry, Scientists, Project Management Skills, Publications, Safety Practices, Collaboration, Method Development, Analytical Method Validation

Industry

Information Technology/IT

Description

ABOUT THE JOB

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.
Sanofi is seeking a highly motivated individual to join our analytical group as a Chromatography Principal Scientist. The group is part of the synthetic platform within Global CMC Development with focus on small molecules that is striving to become an industry leader in the development of transformative medicines.
The primary responsibility of this position is to provide analytical support to the chemistry teams and to develop analytical methods mainly on small molecules using equipment including HPLC, UHPLC, GC, and potentiometry.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

BASIC QUALIFICATIONS

  • A Master’s degree or equivalent in Analytical Chemistry or related field with a minimum of 8ears, 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 experiences in method development using HPLC/UPLC and GC
  • Experiences 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

How To Apply:

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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
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