Sanofi
Analytical Principal Scientist
Sanofi, Cambridge, Massachusetts, us, 02140
Analytical Principal Scientist
Location: Cambridge, MATime Type: Full timePosted on: Posted 3 Days AgoAbout the JobWe 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?Sanofi is seeking a highly motivated individual to join our analytical group as a principal scientist. The group is part of the synthetic platform within Global CMC Development that is striving to become an industry leader in the development of transformative medicines.The primary responsibility of this position is to provide and coordinate analytical support to the chemistry teams and to ensure the timely completion of analytical deliverables. This position is onsite and is based in Cambridge, Massachusetts, USA.Key ResponsibilitiesWorking with project team members and other scientists to develop analytical strategies that meet the evolving needs of projectsDevelop specific and robust analytical methods using equipment including HPLC, UHPLC, GC, TLC, and potentiometry and be responsible for validating the methods when necessaryCoordinate the analytical work for projects this role is responsible forEnsure the appropriate allocation of resources on projects in accordance with the priority of the projects and studiesRepresent the analytical group in late development CMC projectsEnsure timely completion of analytical deliverables (e.g., drugability assessment, specifications, stability program, reference substances, etc.)Author or review analytical development technical reportsEnsure good communication and cooperation among different functional groups, including CMC Dossier, Regulatory CMC, Research Platform, and ManufacturingPromote networking with internal or external scientific partners including subcontractorsAbout youBasic QualificationsA PhD in analytical chemistry or related field with a minimum of 4 years of working experience in the pharmaceutical/biotech industryExtensive experience in analytical method development and validationAbility to operate independently and to prioritizeFamiliarity with cGMP and regulatory requirements on analytical methodsPrior CMC project management experienceExcellent communications skillsPreferred QualificationsAbility to propose course of action and to provide strong advocacy in CMC team meetingsHaving a record of success in CMC project managementHaving working knowledge of synthetic chemistry and pharmaceutical developmentConsistent record of collaboration with scientists and other stakeholders at external enterprisesAdvanced scientific network in the industry and academiaRecord of patents and publicationsRecord of adhering to and promoting lab safety practicesWhy Choose Us?Bring the miracles of science to life alongside a supportive, future-focused team.Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.Pursue
progress , discover
extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
#J-18808-Ljbffr
Location: Cambridge, MATime Type: Full timePosted on: Posted 3 Days AgoAbout the JobWe 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?Sanofi is seeking a highly motivated individual to join our analytical group as a principal scientist. The group is part of the synthetic platform within Global CMC Development that is striving to become an industry leader in the development of transformative medicines.The primary responsibility of this position is to provide and coordinate analytical support to the chemistry teams and to ensure the timely completion of analytical deliverables. This position is onsite and is based in Cambridge, Massachusetts, USA.Key ResponsibilitiesWorking with project team members and other scientists to develop analytical strategies that meet the evolving needs of projectsDevelop specific and robust analytical methods using equipment including HPLC, UHPLC, GC, TLC, and potentiometry and be responsible for validating the methods when necessaryCoordinate the analytical work for projects this role is responsible forEnsure the appropriate allocation of resources on projects in accordance with the priority of the projects and studiesRepresent the analytical group in late development CMC projectsEnsure timely completion of analytical deliverables (e.g., drugability assessment, specifications, stability program, reference substances, etc.)Author or review analytical development technical reportsEnsure good communication and cooperation among different functional groups, including CMC Dossier, Regulatory CMC, Research Platform, and ManufacturingPromote networking with internal or external scientific partners including subcontractorsAbout youBasic QualificationsA PhD in analytical chemistry or related field with a minimum of 4 years of working experience in the pharmaceutical/biotech industryExtensive experience in analytical method development and validationAbility to operate independently and to prioritizeFamiliarity with cGMP and regulatory requirements on analytical methodsPrior CMC project management experienceExcellent communications skillsPreferred QualificationsAbility to propose course of action and to provide strong advocacy in CMC team meetingsHaving a record of success in CMC project managementHaving working knowledge of synthetic chemistry and pharmaceutical developmentConsistent record of collaboration with scientists and other stakeholders at external enterprisesAdvanced scientific network in the industry and academiaRecord of patents and publicationsRecord of adhering to and promoting lab safety practicesWhy Choose Us?Bring the miracles of science to life alongside a supportive, future-focused team.Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.Pursue
progress , discover
extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
#J-18808-Ljbffr