436 English-speaking jobs in Toulouse

Industrialisation Manager to lead and participate in the industrialisation of PEM fuel cell production. Define and implement production roadmap, design layout, and optimise processes. Select, procure, and commission manufacturing equipment. Develop SOPs, quality controls, and support PLM/MES implementation. Collaborate with R&D on DFM principles. Manage CAPEX planning and lead operations team.

Senior AI Scientist will design, build, and maintain generative AI workflows for drug discovery. Responsibilities include developing AI-driven pipelines, integrating machine learning with physics-based simulations, and implementing AI-based protocols for molecular optimization. Requires a PhD in a relevant field and expertise in deep learning, physics-aware AI, and Python programming.

Population PK/Pharmacometrics Modeler will lead modeling strategies, translate findings into recommendations, and drive integration of analyses in oncology drug development. Requires PhD and 5+ years of experience in population PK modeling, NONMEM proficiency, and experience supporting regulatory submissions.

Manages the link between internal services and IT solutions. Collects, analyzes, and defines data requirements, ensuring quality and availability. Proposes, tests, and implements solutions, collaborating with IT and stakeholders. Contributes to process and tool improvements. Requires 3-5 years of experience in business analysis, data analysis, and project management.

Automotive Embedded Software Engineer to develop next-generation solutions in a FreeRTOS and AUTOSAR environment. Requires experience in Embedded C/C++, Python, automotive software components (MAC/MCAL/CDD), and AUTOSAR architecture.

Build and own the client-facing flow of Sparengine's AI-powered aviation technical records platform. Develop upload, analysis, and deliverable views, integrating front to back with the pipeline.

Drive commercial motion from initial contact to first transaction in the aviation aftermarket. Own outreach, qualify pipeline, and lead prospect calls with technical buyers.

Product Safety & Continued Airworthiness engineer will review in-service events, analyze root causes, and manage hazardous conditions. Responsibilities include providing reporting on rare or critical events and analyzing the implementation of corrective actions.

Senior Scientist Bioreactor Process Design will drive development and tech transfer of biotherapeutics manufacturing processes. Responsibilities include preparing and running bioreactors, serving as a functional area lead for process characterization projects, and communicating experimental plans and data. Requires a Master's degree with 8+ years or Ph.D. with 6+ years experience in bioreactor cell culture, perfusion technology, and CMC sections authoring.

Senior AI Scientist will design, build, and maintain AI workflows for drug discovery. Responsibilities include developing AI-driven pipelines, integrating AI with physics-based simulations, and implementing AI-based protocols for conformational sampling.

Population PK/Pharmacometrics Modeler will lead modeling strategies, develop analyses, and integrate findings into oncology drug development programs. Requires PhD and 5+ years of experience in population PK modeling, NONMEM proficiency, and experience supporting regulatory submissions.

Senior Clinical Pharmacologist to lead clinical pharmacology strategy and oversee study design and execution for oncology, dermatology, and rare disease programs. Requires PhD, MD, or PharmD with 4+ years of industry experience in clinical pharmacology and drug development.

The Runway Safety Product Manager will coordinate ROPS support with Airbus/Airlines, support ROPS operators, and lead analysis of in-service events. The role requires experience in ROPS avionics function and Aircraft Performance Development, as well as strong analytical and communication skills.

This role supports the EGNOS service transition from EGNOS V2 to V3. Responsibilities include tracking development for operation and maintenance, defining and following ESP activities during the V2/V3 transition, and ensuring a smooth transition with minimal service interruption. The role works within the ESA project structure and the EUSPA service management framework.

Lead Statistician for Real World Evidence (RWE) studies. Designs, analyzes, and interprets data from RWE studies. Collaborates with clinicians and regulatory agencies. Requires advanced statistical analysis skills and proficiency in SAS. Minimum 6 years of experience in the pharmaceutical industry or CRO.

Lead Statistical Programmer will design and execute Randomized Controlled Trials (RCTs) and Real-World Evidence (RWE) studies. Develop and validate programs for data analysis, reporting, and visualization. Collaborate with statisticians, data managers, and other stakeholders.

Conducts and supports early toxicology and preclinical pharmacokinetic studies. Follows protocols, prepares study materials, monitors animals, administers compounds, and collects biological samples. Processes data and contributes to study reports. Requires skills in laboratory animal science, pharmacokinetics, and computer proficiency.

Digital Verification Engineer with 3-5 years of experience in ASIC verification. Responsibilities include testbench development, verification component development, and test case creation. Requires expertise in System Verilog, UVM, and digital simulation tools.

Supplier Relationship Manager for Electrical Assemblies within Electrics Procurement. Manage supplier portfolio, negotiate agreements, drive cost reduction, and ensure on-time, on-cost, quality delivery for aircraft families. Requires 5-7 years in Procurement/Sales.

CMC Expert needed for drug candidate development and manufacturing. Responsibilities include synthesis route optimization, scale-up, dossier preparation, and regulatory support. Requires 10+ years in CMC expertise and cGMP experience.