Sanofi
DataSystemAnalyst
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Data System Analyst at Sanofi. Skills: Data System Analysis, Process Management, Cross-functional Coordination, Vendor/Stakeholder Management, Operational Metrics, Resource Planning, Continuous Improvement, Digital Transformation. 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 resolve issues related to data m”
What You'll Achieve.
ensure GMP compliance; enabling the digital transformation initiatives; uphold data integrity standards and ensure audit readiness; Help improve the lives of millions of people globally by making drug development quicker and more effective.
Industry & Context.
troubleshoot data storage; archival; restore functions; resolve issues related to data management systems
Share on-call duties for Environmental Monitoring System (EMS) for GMP equipment.
What They're Looking For.
Must Have
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, 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)
Nice to Have
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
What You'll Do.
Serve as site administrator for the Enterprise Content Management system and commonly used analytical laboratory equipment software applications.
and troubleshoot data storage
and restore functions for the resolve issues related to data management systems in collaboration with IS and external vendors.
and external vendors for the development
and implementation of computer-based system applications.
Provide local IT support for lab infrastructure and equipment software applications.
Support the implementation of connected systems and automated data capture
including electronic signatures
and automated notifications in accordance with GxP requirements.
Serve as a key point person for implementation of systems for equipment lifecycle management
and resource management within the Sanofi laboratory workflow application.
Support implementation of automation initiatives by partnering with the Automation
Digital and IS teams.
Prepare User Requirement Specifications (URS)
Lab Instrument Audit Trails
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.
Serve as the liaison between Operations
and external vendors.
Facilitate training and drive adoption of new digital tools across the team.
Evaluate emerging tools and industry best practices relevant to analytical laboratory operations.
Support change management activities associated with digital transformation initiatives.
How You'll Work.
Team & Collaboration
cross-functional coordination; vendor/stakeholder management; Collaborate with IS, Digital, and external vendors for the development, configuration, and implementation of computer-based system applications.; Support implementation of automation initiatives by partnering with the Automation, Digital and IS teams.; 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.; 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.
Communication Scope
organizational and communication skills; communication skills
Process & Methodology
manage multiple priorities effectively, implementation of systems for equipment lifecycle management, maintenance tracking, and resource management, implementation of automation initiatives, Computer System Validation (CSV) activities, change management activities
Full Job Description
**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
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