- Define & implement processes to ensure the robustness of company's vital function (HR, purchasing, IT, project management, knowledge management, etc.).- Define the architecture, tools and partnership to transform the company into a digital enterprise- Recruit and motivate talent- Manage the company's quality and safety policies

Level of attendees: Master of Pharmacy (Industrial)Topics: Manufacturing 4.0, Data & Knowledge Management, Quality by Design, Statistical Process Control and Pharmaceutical Process Optimization

Mission: to provide data governance and solution to Technical Operations & Supply Chain, and enable their digital transformation - Define data strategy (governance, modeling, quality) and support digital initiatives- Deployment of data and master data provisioning solutions- Partner for Digitalization and Manufacturing 4.0 - BIOVIA Discoverant / Pipeline Pilot expert- Project leader for Data science / Big Data applied on pharmaceutical quality and processes, example: * Stability trending, Analytical Method Performance trending, Statistical process controls (CPV), process comparability* CMO data Management * Digitalization & Process Modelling* Clinical / Process correlation- Management of Process Data Specialist teamSpeaker for multiple conferences: BioIT World, Biovia Community, ManuPharma and morePublication in Pharmacetutical Engineering (ISPE) - Sep-Oct 2017 (Vol.37-N.5)https://ispe.org/pharmaceutical-engineering/september-october-2017/finding-relationships-between-clinical-batch

- Big Data Project Management (for pharmaceutical processes)- Implementation of Data model, Discoverant hierarchies / PRIMR - Implementation of Quality by design and Statistics knowledge (JMP, Discoverant, simca)- Lean 6 sigma yellow belt- SQL / XML / HTML / Oracle databases

- Scientific expertise and technical management in process optimization- Coaching of a technical staff through scientific and people performance management- Chemical, technical and process support to any chemical APIs and intermediates process development and Manufacturing to ensure the success of business critical projects.- New technologies / methodologies studies (equipments and methods)

Batches release of Flucis(r) - Responsible of the production and shipment of 18-FDG in Nancy (France)Site Manager - Local safety responsible (nuclear exploitation)Local responsible of GMPs application and conformityMajor improvement of the process by decrease of failuresManagement of 5 persons (4 technicians - 1 pharmacist)

Process improvement of Vinorelbine synthesis Feasibility test on Raman and NIR on chemicals and biologicals productsIntroduction of statisticals based studies on operating conditions of synthesis

Mathematics, chemistry, physic and cellular & molecular biology teacher.Recruitment of collaborators and reorganisation