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Associate Director, Analytical Science and Technology

Framingham, Massachusetts



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  • Health & Wellness

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

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    Sanofi wants to ensure employees are equipped for financial health, Sanofi provides a competitive 401K Match program and Financial Wel-Being Tools and Programs.

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    Sanofi provides significant Work/Life benefits to help you excel beyond the workday. Including Workplace Flexibility through part‑time, remote work, flex‑time and job share options.

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"At Sanofi, We are guided by a deep appreciation and understanding of what it means to live with a rare blood disorder, and we learn by listening to the community – patients, caregivers physicians, and other healthcare professionals."

Shannon Resetich US Head Rare Diseases & Blood Disorders

"Patients are at the center of all that we do at Sanofi. Our teams are focused on advancing transformational therapies that can address serious unmet needs for people living with rare blood disorders, and expanding global patient access to our medicines."

Mouhamed Gueye US Head Medical Rare Blood Disorders




The MSAT function within Specialty Care Operations (SCO) is responsible for leading technology transfer, implementing control strategy, providing technical process and analytical support, and driving process and analytical lifecycle management (LCM) for biologics drug substance operations. Analytical Science and Technology (AST) is a function of the Sanofi Global Manufacturing Science and Analytical Technology organization. AST is a partner of Process Sciences within MSAT, Biologics Quality, and Manufacturing Departments.

AST provides support to:

  • 2nd generation process development for biologics DS

  • Commercial product and analytical LCM

  • Implementation of digital tools and infrastructure

  • Advancement of analytical automation, high throughput capabilities, and PAT

  • Partner with internal and external functions for technology transfer

  • Develop analytical control strategy and support regulatory filings


  • Work with a global group of engineers and scientists and lead a team to provide timely analytical testing support of upstream and downstream processes for monoclonal antibodies, bispecific antibodies, Fc-, Fab-, and fusion proteins, enzymes, and other recombinant proteins

  • Provide analytical support for MSAT development and pilot-scale projects, attend and/or lead  regular team meetings and updates for, data management, investigations, technical report writing and regulatory filings

  • Support regulatory filings

  • Support analytical method transfer and analytical method qualification studies including projects for internal and external partners

  • Support cGMP manufacturing activities including troubleshooting, major investigations, and life-cycle management for analytical activities

  • Work independently to lead a team of scientists to support routine in process testing

  • Implement high through put testing methods and PAT to support analytical testing

  • Review data in ELN for accuracy and compliance to procedures

  • Identify potential problems and proactively suggest technical solutions based upon analytical expertise and knowledge of product/process; solve assay/analytically related process problems

  • Author method procedures, study protocols, technical reports, and manuscripts for publication; present at internal and external meetings and conferences

  • Supervise lower-level analysts in the execution, design, and interpretation of experiments


  • Bachelor’s degree or Master’s degree or equivalent and 8+ years of experience

  • PhD or equivalent and 6+ years of experience


  • Strong written and verbal communication skills

  • Supervisory experience

  • Highly motivated, organized, detail-oriented and able to work in a fast-paced environment

  • Ability to work well both independently and in a team environment

  • Strong problem-solving, communication and inter-personal skills


  • Ability to work in a laboratory environment

As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities.

According to the CDC, an individual is considered to be “fully vaccinated” fourteen (14) days after receiving (a) the second dose of the Moderna or Pfizer vaccine, or (b) the single dose of the J&J vaccine. Fully vaccinated, for new Sanofi employees, is to be fully vaccinated 14 DAYS PRIOR TO START DATE.  

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.


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.

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