2023 – present : Postdoctorate in Photosynthesis regulation (UPSC – Umeå Plant Science Center)
- I came in Sweden in 2023 to start a project with a cutting-edge Technology (C-TRAP from Lumicks) to measure single-molecule protein-DNA binding of key factor of chloroplast developpement. In this project I add to find innovative solutions to different issues :
- Establish a phenotyping workflow based on high resolution pictures to follow plan developpment after emergence
- Create tools to align DNA sequences and Kymographic data from the C-TRAP technology to avoid supplementary costs and gain efficiency.
2018 – 2022 : PhD in Plant Iron Nutrition and Physiology (University of Montpellier, France – IPSiM lab – INRAe)
- Fundamental research on an unknown protein family involved in Iron excess management. There I developped collaboration skills, how to perform research work from literature and models, experimentation and analysis of data. I acquired a spectrum of competences to work autonomously or in teams to resolve technical and biological challenges in an innovative way.
2015 – 2018 : Master of Science in Plant functional Biology (University of Montpellier, France)
- Theory and Practices in Biochemistry, Molecular Biology, Genetics and Epigenetics Project Management : Hypothesis – Planification – Experimentation – Analysis/Interpretation – Communication.
2012 – 2014 : Higher Technical Diploma in Biotechnology (Cannes, France)
- A 2 year specialization in biotechnology and bioengineering – Lab experience with theory and practices. Biotech processes and their optimization. I acquired all the basics of lab work, and experimental design.
2025 : Certifications (Umeå, Sverige), Svensk Medicin AB,
- Essentials of Regulatory Affairs (RA) and Good Distribution Practice (GDP)
Comprehensive training on relevant regulations and guidelines to fully understand the requirements in submitting new MAs for Human Medicinal Products in Europe. In addition to this – how to optimize the life cycle management through submitting relevant variations and line extensions. The course also included how to maintain the safety in pre- and post-approval phases, as well as understanding the complexity of working in a matrix organization. Comprehensive training on all chapters in the EU-GDP legislation and the practical applications of those, leading to understanding how to gain and maintain a Wholesaler license.Essentials of Regulatory Affairs (RA) and Good Distribution Practice (GDP) Comprehensive training on relevant regulations and guidelines to fully understand the requirements in submitting new MAs for Human Medicinal Products in Europe. In addition to this – how to optimize the life cycle management through submitting relevant variations and line extensions. The course also included how to maintain the safety in pre- and post-approval phases, as well as understanding the complexity of working in a matrix organization. Comprehensive training on all chapters in the EU-GDP legislation and the practical applications of those, leading to understanding how to gain and maintain a Wholesaler license. Skills: Corrective and Preventive Action (CAPA) · Regulatory Affairs · current GMP (2025) · Good Distribution Practice (GDP) · Pharmacovigilance · Marketing Authorisation Application (MAA)
- Good Manufacturing Practices (current GMP)
The GMP training course will provide an introduction and basic training with an overview of the pharmaceutical industry cGMP standards. The course will give a solid understanding of how GMP applies to the validation of medical products, focusing on R&D, production, regulations, guidelines, interpretations, requirements and applications.The GMP training course will provide an introduction and basic training with an overview of the pharmaceutical industry cGMP standards. The course will give a solid understanding of how GMP applies to the validation of medical products, focusing on R&D, production, regulations, guidelines, interpretations, requirements and applications. Skills: current GMP (2025) · Risk Assessment · Documentation · Quality Management
- ISO 17025:2017 Laboratory Management Systems, Alison
Comprehensive course about laboratories standardisation and legislation framing the activities of testing and calibration laboratories
Alexis Brun 