Job Title: Data System Analyst

• Location: Framingham, MA

About the job

This position resides within the Operations group, which is part of the Global CMC Development organization and is responsible for supporting equipment management and qualification to ensure GMP compliance. In addition, the group plays a key role in enabling the digital transformation initiatives within the Bioanalytics teams at Sanofi in Framingham and Waltham, MA.

The ideal candidate has a strong technical background in computer systems, knowledge of commonly used equipment control software, experience with the implementation of laboratory automation in regulated analytical laboratories, as well as good organization/communication skills. Specifically, as our laboratories advance towards automation, digitalization, and full adoption of enterprise platforms including automated data capture and electronic notebooks.

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

About Sanofi:

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Main responsibilities:

• Serve as site administrator for the Enterprise Content Management system and commonly used analytical laboratory equipment software applications.

• Program, maintain, and troubleshoot data storage, archival, and restore functions for the department; resolve issues related to data management systems in collaboration with IS and external vendors.

• Collaborate with IS, Digital, and external vendors for the development, configuration, and implementation of computer-based system applications.

• Provide local IT support for lab infrastructure and equipment software applications.

Digital Transformation & Automation

• Support the implementation of connected systems and automated data capture, including electronic signatures, digital audit trails, and automated notifications in accordance with GxP requirements.

• Serve as a key point person for implementation of systems for equipment lifecycle management, maintenance tracking, and resource management within the Sanofi laboratory workflow application.

• Support implementation of automation initiatives by partnering with the Automation, Digital and IS teams.

Compliance & Validation

• Prepare User Requirement Specifications (URS), Impact assessments, Lab Instrument Audit Trails, Deviations, change controls and risk analyses for new or modified equipment/software.

• Author SOPs and training materials related to data management and digital workflows.

• Support Computer System Validation (CSV) activities in partnership with Validation teams.

• Collaborate with Quality Assurance teams to uphold data integrity standards and ensure audit readiness.

• Share on-call duties for Environmental Monitoring System (EMS) for GMP equipment.

Cross-Functional Collaboration

• Serve as the liaison between Operations, Validation, QA, Digital/IS, and external vendors.

• Facilitate training and drive adoption of new digital tools across the team.

Modernization & Continuous Improvement

• Evaluate emerging tools and industry best practices relevant to analytical laboratory operations.

• Support change management activities associated with digital transformation initiatives.

About you

Main Qualifications:

• Master's Degree in Biology, Chemistry, Biochemistry, Analytics Chemistry, data management, Laboratory Informatics, Information Systems / Information Technology or related and >2 years of relevant experience, or Bachelor's Degree in Biology, Chemistry, Biochemistry, Analytics Chemistry, data management, Laboratory Informatics, Information Systems / Information Technology or related and >4 years of relevant experience.

• Minimum 3 years of experience in a cGMP environment

• Strong organizational and communication skills with the ability to manage cross-functional stakeholders.

• Ability to work independently and manage multiple priorities effectively.

• Demonstrated experience with laboratory data management systems (ECM, or equivalent).

Preferred Qualifications:

• Experience with Biovia automated laboratory workflows or equivalent laboratory digitalization platforms

• Familiarity with CSV principles and regulatory frameworks (FDA 21 CFR Part 11)

• Knowledge of data integrity requirements in a GMP environment

Why 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.

• Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.

• Help improve the lives of millions of people globally by making drug development quicker and more effective.

• Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.

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.

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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.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.

North America Applicants Only

The salary range for this position is:

$85.500,00 - $123.500,00

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.