Digital R&D Product Owner
Framingham, 麻薩諸塞州沃尔瑟姆, 麻薩諸塞州 Permanent 发布于 Mar. 16, 2026 申请截止于 Jun. 22, 2026 Salary Range USD 133,500.00 - 192,833.33
Job title: Digital R&D Product Owner
Location: Framingham, MA
About the Job
As Digital R&D Product Owner within our Digital team, you will be part of the iCMC Digital Transformation, a global top initiative that aims at building competitive CMC capabilities and enabling a digital continuum for R&D and M&S data. This is a unique program implementing an ambitious Digital Transformation across process development activities in R&D and M&S, with over 2,500 users across 10+ countries.
The iCMC Digital Transformation initiative is implementing cutting-edge digital technologies to build our next generation of data centralization and data consumption platforms, including paperless CMC labs with end-to-end automated data flows to improve productivity and cycle times, digitized intra- and inter-laboratory workflows to ensure data accessibility and integrity for GMP and non-GMP labs, advanced analytics to optimize key CMC activities leveraging AI/ML agents and modeling platforms, and a foundation for a Digital Continuum from research to development to manufacturing for all our products and processes.
The Digital R&D Product Owner for end-to-end GMP analytical data flows will own, deliver, manage, and optimize the digital solutions for GMP R&D analytical labs, from lab instruments to data capture, data categorization, and data visualization, until its transfer and/or interfacing with Manufacturing, Quality Management, and R&D QC LIMS as part of Sanofi's Digital ecosystem.
Business processes covered include end-to-end workflow for GMP-compliant analytical (DS/DP) laboratory solutions across Sanofi's R&D Bioanalytics, Synthetics, Vaccines/mRNA, and MSAT teams, including generation of Certificate of Analysis and Stability Reporting. This important role will drive digital transformation globally, accelerating analytical workflows while ensuring regulatory compliance and delivering measurable value to patients.
Join the digital engine driving Sanofi’s transformation - where AI, automation, and bold experimentation power faster science and smarter decisions. Here, you’ll help build the first biopharma company powered by AI at scale.
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
Product Strategy & Delivery
Be accountable for ensuring high-quality of E2E data flows delivered for GMP analytical labs from lab instruments to data capture, data categorization and data visualization, until its transfer and/or interfacing with Manufacturing, Quality Management and R&D QC LIMS systems part of Digital ecosystem.
Ensure features developed are aligned with core products strategy & best practices, data flows architecture and aligned with Digital strategy.
Manage complete product lifecycle from ideation through retirement, including E2E support of the product implementation with Agile teams and/or support teams in a GMP compliance context
Develop roadmaps aligned with R&D priorities and regulatory requirements
Identify inter dependencies with other GMP Products (ex: QC LIMS, LES) and manufacturing systems & work closely with manufacturing team, and digital M&S to smooth tech transfer between R&D and Manufacturing & bridge analytical development and manufacturing scale-up
Accountable for building robust interfaces between analytical systems and manufacturing platforms working closely with Technical delivery teams and Digital Architecture
Prepare & facilitate stage gate for your product as part of the Digital R&D governance.
Business stakeholders Management & partnership:
Work closely in partnership with R&D analytical labs teams across Sanofi's R&D Bioanalytics, Synthetics, Vaccines/mRNA, and MSAT organizations to ensure digital solutions proposed are meeting users’ needs
Work closely with Digital R&D product teams & Delivery engines teams to ensure equipment connectivity, methods development, data integration and visualization as well as interfaces are delivered on a timely basis and high quality.
GMP Compliance & Quality
Accountable for data integrity, traceability, and GxP compliance throughout the analytical-to-manufacturing pipeline
Ensure digital solutions meet GMP, GLP, and regulatory standards (FDA, EMA, ICH)
Drive data integrity, traceability, and ALCOA+ principles in all digital workflows
Partner with Quality Assurance, Regulatory Affairs, and Digital Risk & Compliance teams on validation strategies
Maintain audit readiness across all analytical systems
Establish governance frameworks for cross-product integration and data exchange
About You
Education & Experience
Bachelor degree in computer sciences or engineering or Life Sciences/ Bioprocess Engineering/Chemical Engineering or related field.
5+ years of pharmaceutical analytical development experience in GMP, with at least 3 of those years as a Product Owner or Product Manager
Technical Expertise
Deep understanding of GMP/regulatory requirements and pharmaceutical quality systems
Knowledge of laboratory automation, LIMS/ELN systems, and analytical data management
Core Skills
Agile Methodology: Scrum, Kanban, product development
Knowledge or experience on Digital Product Management or product Ownership
Stakeholder Management: Multi-disciplinary, global teams
Data-Driven Decision Making: Analytics, metrics, KPIs
Business Acumen: Strong pharmaceutical R&D operations knowledge
Quality Mindset: Commitment to excellence in regulated environments, experience in Change Control processes and system interacting with Quality team
Nice to have Qualifications
Experience with Waters, Agilent, Thermo Fisher analytical platforms
Vaccines, mRNA, or biologics analytical development background
Cloud platforms (AWS, Azure) and modern data architecture familiarity
Expertise in analytical methods (HPLC, LC-MS, spectroscopy, bioanalytical assays)
Agile/PMP certification
Why Choose Us:
Bring the miracles of science to life alongside a supportive, futurefocused 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.
Join the digital force behind Sanofi’s AI-powered pipeline, where Expert, Generative, and Snackable AI accelerate the discovery, development and delivery of breakthrough treatments to patients.
Help reduce time from discovery to commercialization, delivering life-changing medicines to patients faster than ever.
Join a workplace where diversity, equity, and inclusion are at the core, with Employee
Resource Groups and leadership programs that celebrate every voice.
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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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.
追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
在美国的职位
加入我们的美国团队。我们将为您提供专家指导和培训平台,从而帮助我们营造良好的企业文化。我们鼓励您以饱满的热情和充沛的精力投入到工作中,然后发挥自身能力推进药物和疫苗的研发,同时将研发到临床治疗的时间减半。
体验可能性
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Cambridge Crossing
We're bringing together 2,500 people from across our organization — R&D, Medical, Commercial and Global colleagues all working to realize the power of collaboration.
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Innovation in Action
Our flexible lab of the future will transform how we conduct research, while our innovation center will be fully integrated with existing R&D locations.
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Sanofi’s AI Centre of Excellence in Toronto
The Centre is focused on using leading technologies to develop world-class data and artificial intelligence (AI) products to create value for the health sector.
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Sanofi Canada's Philanthropic Efforts
By chasing the miracles of science to improve people’s lives, we surprise ourselves with what we can achieve. Our team is humbled by the impact our efforts make.
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Sustainable and Green
Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.
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我们的办公地点
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勇敢追梦,奔赴美好未来
想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。
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您和我们相互依存,共同成长
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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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我们的人与文化
我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。
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为什么选择我们?
我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。