424 English-speaking jobs in Toulouse

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.

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.

Pierre Fabre Pharma seeks an experienced Head of Translational Dermatology to drive scientific strategy and excellence across innovative dermatology drug discovery and development programs. This role reports to the Head of Translational Research and leads dermatology clinical development programs, advancing and expanding the portfolio from First-in-Human through Phase II.

Lead Statistical Programmer will design, execute, and analyze RCTs and RWE studies. Develop and validate programs for data analysis, reporting, and visualization. Collaborate with statisticians, data managers, and other stakeholders. Requires a Master's Degree or higher in Statistics and 6+ years of experience in the pharmaceutical industry or CRO. Proficiency in SAS and R programming languages is required.

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.

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.

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.

PK/PD Scientist to support oncology, dermatology, and rare diseases drug discovery. Provide strategic input for compound selection, study design, and program strategy. Characterize exposure-response relationships and support dose optimization. Integrate PK, PD, and biomarker data for translational predictions. Contribute to IND enabling packages and early clinical strategy.

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.

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 Business Owner will lead the refactoring of a Detailed Functional Specification (DFS) authoring tool, driving strategic business value and unifying system engineering processes.

Airbus seeks an A400M Flight Management System (FMS) Design Work Package Leader to lead the definition and design of next-generation FMS standards. The role involves liaising with stakeholders, managing suppliers, and coordinating with multidisciplinary teams. Requires a background in engineering with experience in system design, avionics, and flight management.

Oversee V&V activities and define deployment strategies for Flight Control Systems across Airbus programs. Ensure design and V&V methods are robust for IFCS program and future certification challenges.

Leads complex Export Control projects and develops digital business applications to ensure compliance within Airbus's integrity culture. Oversees a team of technical professionals and manages the full lifecycle of products, applications, or services. Requires 7+ years of IT experience, including people management, and expertise in ITAR/EAR requirements and classification.

Mechanical Inspector will travel to supplier facilities to perform visual and dimensional inspections on parts, assemblies, and sub-assemblies.

Develop and maintain software systems for autonomous satellite operation, improving reliability and scalability. Build tools and systems to enable effective integration and operation on Loft's satellite platform. Scale satellite operations software to support a growing fleet. Contribute to SatDevOps Academy and serve as a rotating Flight Director.

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.

Translational PK/PD Modeler will develop and apply advanced models to guide oncology drug development decisions. Requires PhD and 5+ years experience in preclinical/translational PK/PD modeling. Expert knowledge of oncology-relevant PK/PD models and proficiency in programming and modeling software is essential. Strong communication and collaboration skills are needed to influence cross-functional teams.

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.