674 English-speaking jobs in Occitania

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.

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.

Global Content Operations & Localization Manager will establish and manage an efficient localization pipeline for Royal Canin's digital platforms. This role will partner with regional and local teams, manage translation vendors, and drive the adoption of Translation Management Systems to ensure high-quality content for pet owners worldwide.

Global Utility Engineer will develop and own Royal Canin Utilities Standards for various systems. Responsibilities include managing site utility installations, developing project budgets, and leading conversion/efficiency projects to support sustainability goals. Excellent communication and project management skills are required.

Senior Product Designer to lead the full design lifecycle, from research to iteration. Expert-level Figma skills required. 6+ years of experience as a Senior Product Designer with a background in both product and agency environments.

Global Q&FS Distribution Quality & Traceability Specialist will lead compliance initiatives, standardize processes, and enhance traceability capabilities. Requires a B.S. or M.S. in Food Science, Quality, or Supply Chain with 5-10 years of experience in QFS Management or Supply Chain. Must have familiarity with ISO 9001, ISO 22000/FSSC, or BRC Storage & Distribution standards and proficiency in WMS, Agnostic, and SAP.

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.

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.

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.

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 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.

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.

IT Support Specialist will provide Level 1 and 2 support to Toulouse users, handle IT requests, and manage user access. Responsibilities include troubleshooting network issues, onboarding/offboarding, training users, and maintaining IT equipment. Requires 2+ years of IT experience, strong problem-solving skills, and proficiency in English.

The University of Applied Sciences seeks a Professor UAS in Food Chemistry (80-100%) to teach, conduct research, and collaborate with industry partners. Expertise in food analytics, process-induced-chemical changes, and modern analytical techniques is required. PhD in Food Chemistry, Analytical Food Science, or a related field is necessary. Fluency in English is required, French and German proficiency are a plus.

Independent recruiters can access live global vacancies, submit candidates, and earn $3,000-$11,000 per successful placement.

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

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.

Lead Statistician for clinical trials, designing studies, analyzing data, and collaborating with clinicians and regulatory agencies. Requires advanced degree in statistics, 6+ years experience in pharmaceutical industry, and proficiency in SAS.

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.