79 English-speaking jobs in Occitania

This role is for a Cariste Manutentionnaire Level 1. The position involves 100% handling duties with specific shift schedules Monday through Friday.

Lead dermatology drug discovery programs, shaping research strategies from early discovery through early clinical development. Requires PhD or MD/PhD with 5-10 years of pharma/biotech experience.

Executive Reward and Labor Law Specialist needed to manage legal and contractual processes for Executives (Band III+). This role ensures compliance with French and international labor law across the executive lifecycle.

Lead global packaging technology implementation for wet food, covering primary, secondary, and tertiary packaging. Develop R&D specifications for DRY & WET products across the global manufacturing network.

Lead global packaging technology implementation for wet food, covering primary, secondary, and tertiary packaging. Develop R&D specifications for DRY & WET products across the global manufacturing network.

Lead global implementation of new raw material, process, and product in the WET food network. Develop R&D specifications for manufacturing standards and new technologies. Requires 5+ years in food technology development.

Lead global DRY Technology implementation for new materials, processes, and products across the manufacturing network. Develop and define R&D specifications for DRY product manufacturing. Requires a science/engineering degree and 5+ years in food technology development.

Lead global implementation of new raw material, process, and product in the WET food network. Develop R&D specifications for manufacturing standards and new technologies. Requires 5+ years in food technology development.

Scientific IT Service Manager to co-lead the delivery and improvement of scientific IT services. Responsibilities include managing service lifecycles, supporting applications like LIMS/ELN, and ensuring compliance. Requires a relevant degree and 5+ years in scientific IT service management.

Senior AI Scientist-Molecular Discovery to design and maintain generative AI workflows for drug discovery. Lead ML methodologies for chemical space exploration and molecular optimization in oncology. Requires PhD and expertise in deep learning, diffusion models, and Python.

Lead European Supply Planning operations, driving the 36-month supply plan and optimizing MRP. This role requires 7-10 years in Supply Chain Planning, team leadership, and expertise in planning governance.

eTMF Specialist manages the electronic Trial Master File system for global clinical trials, ensuring regulatory compliance and quality control. Requires 5+ years in clinical documentation management, with 3+ in eTMF roles, and experience with Veeva Vault.

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.

Lead Statistical Programmer needed for RCT and RWE studies. Requires 6+ years in pharma/CRO, expertise in SAS/R, and CDISC (SDTM/ADaM). Must collaborate across teams.

Senior scientific and strategic leadership role shaping oncology R&D strategy and leading partnerships. Requires PhD in life science, cancer biology expertise, and knowledge of the pharma R&D value chain.

Lead the Group's Global Total Rewards strategy and People Analytics. Govern compensation frameworks, job architecture, and benefits across all entities, ensuring data-driven, harmonized processes. Requires 10-15 years in Global Rewards or People Analytics.

This role involves designing and integrating high-voltage (HV) systems and grid connection interfaces for utility-scale energy projects. Responsibilities include ensuring compliance with grid codes and developing HV system designs.

This role involves defining and controlling process validation, IT application, and equipment qualification plans. The position requires leading a team and overseeing the qualification/validation process within a pharmaceutical production site.

Design and develop turbopump components for advanced rocket engines. Responsibilities include 3D modeling in CAD, technical documentation, and analyzing thermomechanical loading. Requires 5+ years in aerospace or turbomachinery.