Junior Bioanalytical Outsourcing Lead - VIE

Junior Bioanalytical Outsourcing Lead - VIE Contract

• Location:
  
  Germany, Frankfurt
• Target start date: 01/04/2026

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.

As Junior Bioanalytical Outsourcing Lead VIE within our Discovery and Translational Science team, you will improve the patient experience by reducing inconvenience and travel, enabling samples to be collected close to the patient, for example thermore, dried spot samples make it possible to do without freezers, which is a major benefit for the environment saving energy and reducing the carbon footprint.

Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

Ready to get started?

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people worldwide. Together, we chase the miracles of science to improve people’s lives.

• Monitor assay development, assay validation and sample analysis processes, ensure timely delivery of quality results in compliance with regulatory guidance.
• Oversee bioanalysis that is performed externally.
• Identify and help onboard vendors for specific analyses, provide advice and support on scientific and technical aspects of analysis where possible.
• Work collaboratively with the Contract Research Organizations (CROs), ensure that all studies are managed in respect to timelines, budget, scientific integrity, and quality deliverables.

• Experience in LC-MS/MS and/or ligand binding assays.

• Excellent communication skills, and the ability to work in a collaborative international environment interacting predominantly in English.
• Awareness of good practice (GxP) and its importance within preclinical and clinical trials.
• Ability to multitask.
• Good organisational skills.

• Master’s degree in biology, chemistry, pharmacy, or related disciplines with a good understanding of bioanalytical technologies.

• Fluent English (written and verbal).

• Be part of a pioneering biopharma company where patient insights shape drug development.
• Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.
• Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.
• Help improve the lives of millions of people globally by making drug development quicker and more effective.
• Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
• Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
• Achieve genuine work-life balance in a supportive R&D environment.