As part of Lorraine Université d'Excellence Initiative (LUE), I support researchers in the emergence and implementation of 3 research programs addressing major societal challenges (health, digital and social transitions): 1/ Health: an interdisciplinary research program “LIFE TRAVEL” focusing on the challenges of aging and the impact of the accumulation of co-morbidities on life trajectories 2/ AI and social sciences: a project "INSIGHT" focusing on the automatic processing of data expressed in natural language in context 3/ Societal transitions: a center of expertise "CELEST” exploring interdisciplinary and cross-disciplinary collaborative research around the transition of scientific practices, the transition of territories as well as that of public policies.

IMPACT GEENAGE (2,5 M€, 10 multidisciplinary partners): a translational research project stemming from LUE “Lorraine Université d’Excellence” which aims to produce new strategies of diagnosis and management of healthy and pathological ageing. + Ensure an operational piloting of the project and the partners with the support of the competentdepartments of the University of Lorraine and the involved laboratories+ Ensure that the project remain on schedule and within budget, is appropriately resourced, andmeet quality standards according to SOPs, and/or other requirements.+ Prepare, edit, and update project timelines and documentation (i.e. required forecasting,budget, deliverables, reports, agendas, minutes, tracking sheets, etc.) to ensure successfulexecution and completion of outlined deliverables.+ Coordinate communication amongst Steering Committee members. Organization of meetings,workshop, and preparing documentation for meetings and report on progress to the SteeringCommittee.

+ Review and validate promotional, institutional and educational materials to healthcare professionals and patients for OTC products in compliance with local rules and practices to support business objectives + Perfom submission of promotional materials to ANSM in respect of defined planning + Ensure follow-up and traceability of promotional materials+ Review and validate of labelling for medical products + Provide training and ongoing education to Weleda employees (including sales reps, marketing, medical and other relevant roles) with respect to regulatory processes, ANSM regulations + Ensure quality documents are defined, created, maintained and implemented. + Ensure anti-gift law (DMOS) compliance by reviewing and validating promotional and partnership operations with HCP(s): congress, invitations, honoraria, agreements, grants …) + Manage declaration to Professional Committees and ensure data availability for disclosure “French sunshine act” + Strategic analysis for executive board and marketing/medical departments on legal or regulatory topics, as necessary (taxation, borderline products...)+ Play an active role in public affairs concerning reimbursement issues.

+ Review regulatory documentation and prepare regulatory submissions in area of expertise, as appropriate for Phases I & II clinicals trials (study protocol, study amendment, informed consent document and dossier for Ethics Committee [EC]) + Provide technical input consultancy and technical review for regulatory matters+ Interact with Regulatory Authorities (ANSM, EC...) + Interact with internal and externals clients in area of expertise + Keep up-to-date with regulatory knowledge, trends, and developments in the area of expertise.

+ Manage european cosmetic dossiers for fragrances and cosmetics products (Gucci, Escada, Rochas...)+ Ensure and provide international registration documentation as needed for export + Review of cosmetic product labelling according to european & international requirements+ Responsible for customer service and follow-up of cosmetovigilance cases.

+ Prepare legal documentation relating to the risk of BSE transmission to human beings by use of cosmetic products (Bovine Spongiform Encephalopathy) + Analysis of the consequences of the implementation of the seventh amendment of the European Directive n° 76/768/CEE for Cosmetic Industry+ Legal qualification of health products within the area of “borderline products”+ Participation to the working group which evaluate the requests relative to “VISA PP” (French specificity concerning the review of health claims).