Job Title: Reliability and Methods Specialist
Location: Framingham, MA
About the Job
Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.
Our team oversees the configuration, optimization, and governance of the CMMS platform, enabling data-driven decision-making and proactive maintenance strategies. We also manage the full lifecycle of MRO inventory—from procurement and storage to usage and replenishment—ensuring that the right parts are available at the right time, without excess or waste.
With a strong focus on GMP compliance, asset reliability, and continuous improvement, we collaborate closely with engineering, quality, and operations to support safe, efficient, and uninterrupted manufacturing. Our commitment to excellence helps safeguard product quality and patient safety, while driving cost-effective maintenance practices across the organization.
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:
Administration and maintenance of Hexagon EAM master data including assets, equipment hierarchies, locations, PM schedules, and spare parts.
Ensures CMMS data complies with pharmaceutical industry regulations
Perform regular data audits and cleansing to ensure accuracy, completeness, and traceability.
Generate reports and dashboards for KPIs such as PM compliance, work order backlog, MTTR, and asset performance.
Train users on Hexagon EAM functionality, workflows, and data entry standards.
Support annual fixed asset audit to align site Fixed Asset Registry with CMMS equipment catalog.
Support periodic alignment of CMMS equipment catalog with Veeva/Qualipso equipment registry
Key Involvement in Decision -Making Process
D: CMMS master data audit and accuracy
A: Equipment updates, activation, deactivation
A: Hierarchy and master data input for project
About You
Local Specificities
Expected Experience:
Associate’s degree in Data Base management, industrial maintenance or related fields.
2+ years of experience in Data Base management, industrial maintenance or similar areas.
Experience with Hexagon EAM or similar CMMS in a GMP-regulated environment.
Familiarity with FDA regulations, validation principles, and data integrity requirements.
Proficiency in Excel, data analysis, and report generation.
Excellent attention to detail, organizational, and communication skills.
Preferred Skills:
Experience with asset hierarchy development and maintenance strategy optimization.
Familiarity with GMP procedures is highly preferred
Familiarity with SQL, Cognos Reports, or BI tools for CMMS reporting.
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.
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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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:
$84,000.00 - $121,333.33All 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.