Full-Time

Data Scientist

Deadline 8/28/26
Sanofi

Sanofi

10,001+ employees

Global pharma company; vaccines and R&D

Compensation Overview

€48k - €64k/yr

+ Short-term incentive + Collective variable compensation

Lyon, France

Hybrid

Three days in the office and two days working from home per week.

Master's, PhD

Category
Data & Analytics (1)
Required Skills
LLM
Streamlit
Power BI
Python
Data Visualization
Data Science
Neural Networks
Forecasting
InfluxDB
Apache Spark
Machine Learning
Apache Kafka
RAG
Version Control
Tableau
AWS
Seaborn
DevOps
Databricks
Plotly
Data Analysis
Google Cloud Platform

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Requirements
  • Hands-on experience working with Internet of Things data, sensor streams, or time-series data.
  • Demonstrated experience applying machine learning to real-world problems, ideally involving signals or temporal data.
  • Experience developing deployable code and taking models to production in an agile environment.
  • Experience working with messy, inconsistent, or legacy real-world data.
  • Knowledge of the pharmaceutical or chemical domain, including manufacturing processes, GxP, or laboratory environments, is advantageous.
  • Excellent written and verbal communication skills.
  • Experience working with multiple teams to drive alignment and results.
  • Strong Python skills and familiarity with at least one database system, particularly time-series databases such as InfluxDB or TimescaleDB.
  • Solid command of time-series methods, including forecasting, anomaly detection, and signal processing, applied to streaming data.
  • Working knowledge of streaming and real-time data technologies such as Kafka, Spark Streaming, MQTT, or similar technologies.
  • Strong machine learning foundations, including supervised learning, unsupervised learning, and deep learning, with understanding of the underlying theory.
  • Comfort working in cloud and high-performance computing environments such as Amazon Web Services, Google Cloud Platform, Databricks, and Apache Spark.
  • Knowledge of software engineering practices, including version control, testing, continuous integration, continuous delivery, and orchestration.
  • Experience with data visualization tools such as Power BI, Tableau, Streamlit, Plotly, or seaborn.
  • Experience handling sensitive data in critical environments such as healthcare.
  • A Master's degree or PhD in engineering, computer science, mathematics, physics, statistics, or a related quantitative discipline with strong coding skills.
  • English and French language skills.
Responsibilities
  • Partner with business teams to understand requirements and translate them into technical solutions with a good degree of autonomy.
  • Own the ingestion, cleaning, and harmonization of Internet of Things and sensor data from connected, streaming, legacy, manual, and inconsistent sources.
  • Design and deliver time-series models for forecasting, anomaly detection, and monitoring on streaming sensor data to improve manufacturing performance and quality.
  • Design, build, and support real-time and streaming data pipelines with engineers and machine learning operations teams, and help bring legacy sites to a usable state.
  • Write highly optimized, production-ready code and take models from experimentation through deployment.
  • Scope, define, and deliver artificial intelligence-based data products end to end using data analysis, visualization, and storytelling.
  • Be accountable for the robustness of delivered artificial intelligence solutions by applying responsible artificial intelligence practices, including monitoring, explainability, trustworthiness, and ethics.
  • Contribute to and help raise standards within the global data science community of practice.
  • Support junior data scientists and analysts through informal guidance and code review.
Desired Qualifications
  • Familiarity with large language models, Retrieval-Augmented Generation, or agentic artificial intelligence workflows.
  • Background in chemical or process engineering, control systems, or signal processing.

Sanofi is a global pharmaceutical and biotechnology company that develops, manufactures, and sells prescription medicines, over-the-counter products, and vaccines. Its products span immunology, oncology, rare diseases, and vaccines, addressing unmet medical needs through a strong focus on research and development. Sanofi's core product model relies on large-scale R&D, strategic partnerships, and licensing to bring new therapies to markets, with revenue generated from product sales and collaborations. The company differentiates itself by leveraging its global reach, diverse portfolio, and emphasis on patient-centric solutions, safety, and quality to navigate regulatory environments in developed and emerging markets. The company’s goal is to improve health outcomes and quality of life for people worldwide by delivering innovative treatments and vaccines that meet unmet medical needs.

Company Size

10,001+

Company Stage

IPO

Headquarters

Paris, France

Founded

1973

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Simplify Jobs

Simplify's Take

What believers are saying

  • Q2 2026 sales rose 17.8%; Dupixent topped €5.2 billion for the quarter.
  • July 30 upgraded 2026 guidance to around 10% sales growth, with higher EPS.
  • August 4 MenQuadfi infant approval widens vaccine reach; Nexviazyme's June phase 3 readout strengthens pipeline.

What critics are saying

  • Dupixent faces tougher H2 2026 comparisons, threatening growth after the €5.2 billion quarter.
  • Cenrifki carries liver injury risk; strict monitoring can slow adoption and invite liability.
  • Dupixent concentration and Regeneron's November 2024 lawsuit threaten Sanofi's core growth engine.

What makes Sanofi unique

  • Dupixent and partnered launch engine generate repeatable immunology cash flows across geographies.
  • Sanofi converted 2026 approvals for Sarclisa Escena, Wayrilz, and Cenrifki into launches.
  • Paulo Fontoura's September 1 R&D mandate centralizes translational science and regulatory execution.

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Benefits

Health Insurance

Professional Development Budget

Parental Leave

Company News

Business Wire
Aug 13th, 2026
Epicrispr Biotechnologies Closes $90 Million Oversubscribed Series C Financing to Advance First-in-Class Epigenetic Therapy Toward Pivotal Studies in FSHD

Epicrispr Biotechnologies Closes $90 Million Series C Financing to Advance First-in-Class Epigenetic Therapy Toward Pivotal Studies in FSHD

Morningstar
Aug 12th, 2026
InduPro raises $77M Series B, doses first patient in Phase 1 trial of bispecific ADC for lung cancer

InduPro has closed a $77 million Series B financing round and dosed its first patient in a Phase 1 study of IDP-001, its lead oncology programme. The biotechnology company is developing IDP-001, a bispecific antibody-drug conjugate targeting EGFR and a novel tumour-associated proximity antigen, for treating advanced squamous non-small cell lung cancer and other solid tumours. The Column Group led the financing round, with participation from Vida Ventures, MRL Ventures Fund, Emerson Collective, Euclidean Capital, Solasta Ventures, Sanofi, and Eli Lilly and Company. Proceeds will support Phase 1 clinical development and early proof-of-concept data generation for IDP-001, whilst advancing InduPro's broader preclinical pipeline. InduPro uses a proximity-guided platform to map protein spatial relationships on cell surfaces for discovering selective co-target pairs.

FinancialContent
Jul 24th, 2026
Scribe Therapeutics prices upsized $129M IPO at top of range

Scribe Therapeutics, a clinical-stage biotechnology company developing in vivo CRISPR technologies, has priced its upsized initial public offering at $15.00 per share, the high end of its range. The company is offering 8,580,000 shares, expecting to raise $128.7 million in gross proceeds before fees and expenses. Scribe has also granted underwriters a 30-day option to purchase up to 1,287,000 additional shares. The shares are expected to begin trading on the Nasdaq Global Market on 24 July 2026 under the ticker symbol "SCTX", with the offering closing on 27 July 2026. Additionally, Scribe has agreed to sell 500,000 shares at the same price to Sanofi in a concurrent private placement. Leerink Partners, Goldman Sachs, Guggenheim Securities, and Wells Fargo Securities are serving as joint book-running managers.

Associated Press
Jul 10th, 2026
Sanofi's Sarclisa Escena approved in US as first anticancer drug delivered via on-body injector

The US Food and Drug Administration has approved Sanofi's subcutaneous Sarclisa Escena for treating multiple myeloma, making it the first anticancer treatment administered through an on-body injector. The therapy uses Enable Injections' CirCLIQ device, which delivers the drug automatically with a retractable 30g needle. The approval was supported by the IRAKLIA phase 3 study, which demonstrated that Sarclisa Escena delivered via the on-body injector provided similar efficacy and safety compared to intravenous infusion, with significantly shorter treatment time and fewer infusion-related reactions. The study showed a 71.1% objective response rate in patients with relapsed or refractory multiple myeloma. More than 70,000 patients worldwide have been treated with Sarclisa-based regimens. The on-body injector aims to reduce physical burden on healthcare providers whilst offering patients greater convenience during treatment.

Yahoo Finance
Jul 5th, 2026
Sanofi appoints Paulo Fontoura as R&D chief to accelerate pharma pipeline transformation

Sanofi has appointed Paulo Fontoura as Executive Vice President and Global Head of Research & Development Pharma, effective 1 September. Based in Paris, Fontoura will oversee the company's innovation engine, spanning research, translational medicine, clinical development, and regulatory affairs. He succeeds Dr Houman Ashrafian, who is leaving to pursue new opportunities. Fontoura brings over 25 years of experience across academic medicine, translational science, and pharmaceutical innovation. The appointment comes as Sanofi drives an R&D transformation whilst progressing its pipeline across multiple therapeutic areas. Separately, MacroGenics confirmed it will receive $24.5 million in regulatory milestone payments from Sanofi following FDA accelerated approval of TZIELD to delay decline in endogenous insulin production in children. Sanofi is a global biopharmaceutical company focusing on immunology, rare diseases, and oncology.