727 English-speaking jobs in Occitania

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.

Satcom Consultant Engineer to support technical studies, feasibility analyses, and procurement of satcom systems (LEO, MEO & GEO). Requires 3-5 years of space sector experience, preferably in satcom, with expertise in satellite link budget analysis and/or payload architecture. Strong communication and presentation skills are essential. Fluent English required.

Lead opto-mechanical development for a next-generation LEO satellite constellation. Design high-precision assemblies, perform analyses, and own designs from engineering units to flight hardware. Collaborate with cross-functional teams and suppliers.

Drive sales area development and achievement of targets. Lead and manage teams across all channels, analyze KPIs, and implement action plans. Conduct performance talks, report area development, and attract, develop, and retain talent. Collaborate with sales team to achieve performance goals and support the roll-out of pricing concepts and brand positioning.

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.

Leads the definition and deployment of a best-in-class Retail & Commercial Excellence model across 45 international markets. Accountable for translating strategy into consistent execution, driving profitable growth and customer engagement. Ensures price positioning, promotion activation, and visibility are delivered in-store. Develops playbooks, training programs, and leads market rollout to drive adoption of Commercial Excellence capabilities. Collaborates with GMs and sales teams to support joint business plans and identify growth opportunities.

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. Expertise in PK/PD study design, analysis, and interpretation, pharmacometric software, and regulatory requirements.

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.

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.

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.

Translational PK/PD Modeler needed for oncology programs. Develop and apply PK/PD models to guide candidate selection, dose optimization, and mechanistic understanding. Collaborate with cross-functional teams and contribute to IND submissions and publications. PhD in a quantitative field and 5+ years of post-PhD experience in preclinical/translational PK/PD modeling required.

Chemical Expert for CMC on a permanent contract at the Toulouse site. Focuses on drug substance development and manufacturing, including synthesis route selection, scale-up, technology transfer, characterization, and support for validation and specification definition.

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.

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

Join Emirates' international cabin crew team. Successful candidates will undergo a 7.5-week training program in Dubai covering safety, service, and Emirates hospitality. Fluency in English, a team player attitude, a minimum of 1 year of hospitality experience, and a Grade 12 education are required. Applicants must meet UAE employment visa requirements and be at least 160cm tall. No visible tattoos are permitted while in uniform.

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.

Leads a team of scientists in cell culture and bioreactor process development, characterization, and validation. Collaborates across the organization to accelerate clinical development timelines and optimize process development strategies. Defines and drives technology development for process intensification and continuous manufacturing. Serves as a Project Team Lead and technical resource for cGMP manufacturing and Process Design. Communicates scientific information and experimental plans to internal and external 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.