Skip to main content

Manager Scientist

Meriden, Connecticut

Sanofi, in the U.S. and Canada, strives to create a diverse and inclusive work environment that empowers employees to drive their careers and be successful. The talent we look for will contribute to the organization in innovative, insightful, and creative ways in order to strengthen our dynamic culture and drive us collectively to make a difference in the lives of patients.

Back to Job Navigation (Overview)

Rewards

  • HEALTH AND WELLNESS PROGRAMS

    Comprehensive coverage including medical, dental, vision, and health and wellness programs.

  • EMPLOYER MATCHING

    Employer matching because Sanofi invests in their employees!

  • PROFESSIONAL DEVELOPMENT

    Sanofi is eager to further your development and expertise in an ever challenging environment.

  • FAMILY SUPPORT

    Sanofi understands the importance of family. We offer a variety of support including maternity/paternity leave.

  • PAID TIME OFF

    Enjoy 3 weeks’ vacation and paid holidays, including company shutdown at the end of every year!

  • WORK/LIFE BALANCE

    Importance of life outside of the office is valued at Sanofi.

Back to Job Navigation (Rewards)

Responsibilities

Manager Scientist
Analytical and Formulation Development

Reports to: Deputy Director Analytical Formulations
Personnel Managed: Analysts, Professionals

Responsibilities: Candidate will contribute directly to the development, improvement, and management of recombinant protein vaccines.  As a member of the Analytical Formulations team, the candidate will lead the development and optimization of analytical assays to characterize vaccine targets, design experiments and studies to trouble shoot and investigate protein stability, and analyze and trend data for vaccine life cycle management.  Candidate will accomplish these tasks in a laboratory setting and through collaborations both internal and external. 

  • Function as a lead and subject matter expert in investigations to support vaccine development and manufacturing.
  • Develop assays to monitor manufacturing processes and characterize proteins and vaccines using both immunological and biophysical methods and techniques such as Enzyme-linked Immunosorbent Assay (ELISA), Bi-layer Interferometry (Octet), Differential Scanning Fluorometry (DSF), Infrared spectroscopy (IR), Capillary Electrophoresis (CE), and Ultra Performance Liquid Chromatography (UPLC).
  • Transfer newly developed assays to the Quality Control and/or Process Development groups as required. 
  • Design and execute studies to evaluate changes to manufacturing processes, equipment and/or site, and to evaluate the stability of novel protein candidates.
  • Identify stability and formulation problems and evaluate potential solutions and improvements independently.
  • Participate on cross-functional teams to manage and facilitate projects.
  • Manage and train analysts on procedures and systems.
  • Adhere to company policies and maintain documentation and records of laboratory data and results.
  • Provide and write status updates, status reports, assessments, development reports, procedures, and publish manuscripts in peer reviewed journals where appropriate.
  • Maintain a knowledge of the scientific literature.
  • Present ideas, concepts, and findings internally and externally and represent the company at national and international scientific conferences.

Education, Qualifications, and Experience/Skills:

  • Ph.D. degree in Biochemistry or relevant field including Biophysical Chemistry, Biology, Biomedical Engineering or combination of experience and training that is equivalent.
  •  2-5+ years of hands on post-doctoral experience in the characterization of vaccines and biologics in a pharmaceutical or biotechnology industry setting preferred.
  • Experience is biophysical and biochemical characterization of proteins and a familiarity with state of the art biophysical and biochemical assays such as DSC, DLS, DSF, Bi-layer Interferometry, and UPLC.  Experience in assay validation is a plus.
  • Familiarity with cGMPs and/or vaccine manufacturing.
  • Experience in managing multiple projects and laboratory personnel.
  • Excellent verbal and written communication skills.

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.

#GD-SP  

#LI-SP   

At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

Jobs for you

View All of Our Available Opportunities

Your jobs

Saved Jobs Recent Jobs

You have not saved any jobs yet

You have not viewed any jobs yet

Join our Talent Community

Join our Talent Network and get Sanofi communications and job alerts delivered to your inbox.

Interested InSearch for a category and select one from the list of suggestions. Search for a location and select one from the list of suggestions. Finally, click “Add” to create your job alert.

  • Medical Scientist, Meriden, Connecticut, United StatesRemove
  • R&D, Meriden, Connecticut, United StatesRemove
  • Laboratory, Meriden, Connecticut, United StatesRemove