Integrated Manufacturing Systems Manager

Job Title Location: Framingham, MA About The Job The Automation and Manufacturing Systems (AMS) group is at the forefront of Sanofi's digital transformation journey, driving operational excellence through innovative technology solutions and smart manufacturing initiatives. As a critical enabler of our global manufacturing network, the team drives the development, implementation, support and maintenance of leading automation strategies, Industry 4.0 technologies, and integrated automation manufacturing systems that enhance production efficiency, ensure product quality, and maintain computerized system regulatory compliance. Working closely with cross-functional partners at the site and global level, the group champions continuous improvement, ensures cybersecurity, and system robustness while fostering a culture of innovation that directly contributes to our mission of delivering life-changing medicines to patients worldwide. Through strategic leadership in automation, digital integration, and manufacturing excellence, the team plays a pivotal role in shaping Sanofi's future manufacturing capabilities and maintaining our competitive edge in the pharmaceutical industry. We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. About Sanofi Were an R&D-driven, AI-powered biopharma company committed to improving peoples 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 lives. Main Responsibilities Develop and execute the site MES master plan.Provide leadership and development of the MES and DHS team.Develop and manage the site MES resource plan. Allocate resources to projects, and leads MES recruitmentPerform routine checks and monitor MES and DHS to ensure smooth operation and support of production schedulesLead and support interface management to maintain MES and equipment integrationLead and provide oversite for configuration of MES, Data Historian, and Kepware systemsEnsure compliance with industry standards and regulationsOptimize production processes through MES implementations.Follow established protocols to verify data completeness, accuracy, and compliance within MES/DHSTroubleshoot system issues to minimize downtime and maintain operational efficiencyMaintain documentation and records in accordance with compliance standardsParticipate in global networks, contribute lessons learned to the networkParticipate in global initiatives when requestedResponsible to understand current global design guidelines and application Key Involvement in Decision-Making Process D: Strategy and Roadmap for site MESD: Decide on immediate troubleshooting steps and corrective actions for minor issuesD/A: MES project prioritization and resource allocationD/A: Process improvement initiatives through MESA: Compliance strategies for MESA: Ensure data accuracy and integrity in data management tasksA/I: Assist with troubleshooting and ensuring smooth interface operationsI: Involved in reporting system issues or trends to managers for strategic decisionsI: Contribute to configuration processes, reporting any issues About You Basic Qualifications Bachelors degree in engineering (Chemical, Electrical, Computer, Industrial, or related discipline), Biotechnology, Computer Science, or related technical fieldMinimum 8-10 years of progressive experience in manufacturing, automation, MES implementation, or manufacturing systems engineering within a regulated industry (pharmaceutical, biotech, medical device, or similar GxP environment)Minimum 3-5 years in a leadership or supervisory role managing technical teamsDemonstrated experience leading strategy, roadmap development, and cross-functional project deliveryExperience in computerized system validation (CSV) and regulatory compliance (FDA 21 CFR Part 11, EU Annex 11, GAMP 5)Professional certifications in MES platforms (e.g., Siemens, Rockwell, Emerson DeltaV), Project Management (PMP), SAP, or Industry 4.0/Smart Manufacturing10-12+ years of total experience in pharmaceutical manufacturing automationExperience working in global or multi-site manufacturing environmentsDirect experience with Sanofi's standard MES platforms and data historian systemsTrack record of leading digital transformation or Industry 4.0 initiativesExperience with cybersecurity frameworks for OT/IT systemsI: Involved in record-keeping and data capture, ensuring documentation aligns with compliance standards 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 its 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 andwellness programs and at least 14 weeks gender-neutral parental leave.Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scaleTransform lives worldwide by delivering life-changing treatments anywhere, anytime. 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. #GD-SG #vhd All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.