Manufacturing Supervisor - Second Shift
From Research and Development to Sales and Marketing, Sanofi offers a wide range of possibilities. Discover our open positions and become a health journey partner.
Do you have what it takes for a successful career with Sanofi?
- Team player
Culture: Play to Win
Health & Wellness
Comprehensive coverage including medical, dental, vision, and health and wellness programs.
Sanofi wants to ensure employees are equipped for financial health, Sanofi provides a competitive 401K Match program and Financial Wel-Being Tools and Programs.
At Sanofi, we demonstrate our commitment to inclusion and diversity through Culture groups and programs. There are many ways to make a difference and connect with other Sanofi employees: including ERG groups and 2 PAID days off to Volunteer.
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.
"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."
"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."
Position Overview/Department Description
Sanofi’s Genomic Medicine Unit (GMU) CMC group is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors, and cell therapy products.
Sanofi is looking for a cell therapy leader with GMP manufacturing expertise to serve as Clinical Cell Therapy Manufacturing Supervisor. This is an exciting opportunity to join Sanofi’s GMU and be part of building the company’s cell therapy manufacturing strategy. The ideal candidate will have expertise in cell therapy manufacturing with a demonstrated track record of successful development-to-clinical product transitions. Creativity, scientific thoroughness, entrepreneurial mindset, and ability to function in a complex environment are essential.
The primary accountability of this role is to enable the manufacturing of cell therapy products for clinical supply, as a cell therapy technical expert for cGMP manufacturing, through providing hands-on technical leadership and operational oversight for a cell therapy manufacturing suite in Framingham, MA. We are looking for a candidate with excellent GMP, scientific, technical, communication, and leadership skills.
The individual will initiate LIRs, OTN and site deviations.
The individual works cross-functionally and in collaboration with internal support departments and Manufacturing suite to develop or update internal policies, procedures or steps, identifies and escalate risks, communicates changes and plan for execution.
Manage, and monitor functional area project and tasks: Campaign support and readiness, MFG process specific change controls, CAPA’s, Laboratory Investigation Reports (LIR), Validation activities.
Advanced technical knowledge of cell therapy manufacturing operations/ process
Working knowledge and experience with Quality Systems including deviations and change controls
Excellent communication skills both verbal and written.
Bachelor’s degree in sciences or engineering discipline with a minimum of 5 years of industry experience or a Master’s degree with a minimum of 3 years of industry experience
Experience with GMP regulations and cell therapy
Experience in GMP documentation and compliance
Ability to operate and thrive in a fast-paced, high-growth environment
Strong skills in change management
Excellent communication skills
Direct experience in cell GMP manufacturing facilities with expertise in CAR-T, NK cell therapy
Involvement in delivering a cell therapy-based product into clinical development
Shift: Sunday-Wed or Wed - Sat, 3:30 PM - 2:00 AM. 10 hours shifts x 4 days a week
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.