About the role
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
- Master's Degree in Biology, Chemistry, Biochemistry, Analytics Chemistry, Bioprocessing, 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, Bioprocessing, data management, Laboratory Informatics, Information Systems / Information Technology or related and ≥3 years of relevant experience. Master's degree students graduating in summer or fall will be considered.
- Minimum 1 year 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.