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Supervisor Genomic Medicine Bioanalytics, CT Flow Cytometry - Second Shift

Framingham, Massachusetts

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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


Position Overview/Department Description

This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Cell Therapy Flow Group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust flow cytometry methods to support in-process, release and characterization testing of different cellular therapy candidates. In addition, the group supports cGMP-compliant release and stability testing of clinical supplies performing both the product-specific as well as compendial methods.

We are looking for a skilled and highly motivated scientist with broad expertise in immunophenotyping and cell sorting method development to join the GMU CT QC Flow group in Framingham, MA.

Overview of role

The primary accountability is to perform and develop flow-based analytical methods, cGMP testing, and validation activities. In addition, the GMU CT Flow Group will be responsible for introducing new technologies and ways of working to enable rapid progression of various early-stage cell and gene therapy candidates into the clinic.

Key Responsibilities

  • Performs all activities in accordance with cGMP requirements and reports discrepancies.  Initiates and complete laboratory discrepancy events within expected timelines

  • Provide and supervise analytical support for manufacturing operations, including qualification of in-process and release methods and assist in tech transfer internally and externally in support of GMP manufacturing and release of clinical material.

  • Acquire a working knowledge of flow cytometry for routine testing, method validation and method transfer process

  • Documents testing activities and results, ensuring completeness and accuracy per cGMP

  • Contributes toward the development, revision, application, maintenance, validation and review of method SOPs.  Initiates and follows up on change request for SOP revision.

  • Ensure high-quality, timely documentation in electronic laboratory notebooks and technical reports which support regulatory filings.

  • Perform assay training and supports qualification of junior analysts

  • Provide technical oversight and manage the workload for a few junior analysts

  • Other duties as assigned

Basic Qualifications

  • Ph.D. in Molecular Biology/Biochemistry/Biology or related discipline or Master’s degree with a minimum of four years of relevant industry experience, or a Bachelor’s Degree with a minimum of six years of relevant industry experience

  • Experience in a cGMP environment and ability to adhere to all appropriate cGMP standards (e.g. invalid result investigations, deviations, and CAPAs)

  • Experience leading a small team

  • Able to follow instructions and SOPs precisely and able to keep accurate and contemporaneous documentation

  • Able to learn new skills rapidly and achieve proficiency.  Detail-oriented with good written and verbal communication skills

  • Ability to solve problems of moderate complexity and troubleshooting as necessary

  • Team player with good interpersonal skills

  • Self-motivated with excellent organization, time-management, and communication skills

Preferred Qualifications

  • Experience authoring SOPs

  • Previous working experience in aseptic techniques and in flow cytometry is required

  • Experience with transferring methods between groups in a cGMP environment

  • Experience with validation and transfer analytical methods

  • Experience in maintenance of GMP laboratory, laboratory equipment, and the status of pipettes and supplies.

  • Experience using Quality by Design (QbD) principles and have used Design of Experiment (DOE) approaches for method development/optimization

At Sanofi R&D North America, we deliver meaningful solutions for patients. We transform science into breakthrough, best-in-class and first-in-class medicines and vaccines. We believe in creating a diverse and inclusive workforce – and workplace – which brings together the collective brainpower of over 2,000 colleagues and provides you with an exciting place to grow and develop. We set the bar high, and we deliver. Join us and together we will build on our trusted legacy of breakthroughs for society. 

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.

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.


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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