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I work on topicsprocess, technicalandespecially mixed, mainly in pharmaceutical and industrial environments. Mydual roleas an industrial pharmacist / mechanical engineer allows me tounderstandboth theprocess, the qualityandregulatory, and the, et les real constraints ofthe equipment. This cross-functional vision allows for a.

Cette vision transversale permet un significant time savings: it facilitates communication between production, quality, maintenance, engineering, and management. Thanks to my hands-on experience, I can engage with operators, technicians, and management to clarify needs and build a concrete response. significatif : elle facilite les échanges entre production, qualité, maintenance, bureau d’études et direction. Grâce à mon expérience terrain, je peux dialoguer avec les opérateurs, les techniciens comme avec l’encadrement, pour clarifier le besoin et construire une réponse concrète.

On the pharmaceutical process side, I support investigation topics, analysis of deviations or complex deviations: identification of probable causes, assessment of quality impact, construction of hypotheses, definition of effective CAPA, support for process validation and equipment qualification (protocol and report writing). My experience particularly covers aseptic environments, lyophilization, filling operations, production equipment, and associated GMP constraints.

Côté technique, j’interviens sur l’analyse d’équipements industriels, la modélisation, la CAO, la conception mécanique, la mise en plan, la préparation de rétrofits, le prototypage par impression 3D et la formalisation de solutions adaptées aux contraintes terrain. L’objectif est de produire des livrables clairs, utiles et directement exploitables par les équipes projet, production, maintenance ou bureau d’études.

My approach is based on a logic of“right first time” : taking the time, from the start, to properly frame the need, understand the constraints, and thus maximize the chances of proposing the optimal and directly usable response while considering the process, regulatory requirements, and the technical realities of the equipment.