• Provide a technical advisory role to teams on several aspects of medical product development across the entire division.• Coordinate with the numerous multidisciplinary teams and the Quality, Manufacturing, Maintenance and Regulatory departments.• Act as a resource person to develop and implement new procedures focused on performance and the effectiveness of work methods.• Manage a team of 21 engineers and their distribution to various parallel and active projects according to their expertise and interests.• Plan the needs of the group and teams according to project and resource forecasts.• Maintain cyclical performance metrics and high employee engagement scores.• Coordinate recruitment, training and performance evaluation activities.• Participate in the development and implementation of human resources projects.Achievements:• Managed the development of the ROSA® Shoulder robotic application including the design of the system and its integration with existing platforms.• Created a team of post-market engineers focused on continuity and commercial expansion activities for existing products• Actively participated in the initiation, development and implementation of a SOLIDWORKS PDM electronic management system for medical instrument specification documents.• Adapted and implemented the SCRUM Agile method for the development of medical instruments complementary to application software to have a uniform workflow with the software and system development teams.• Provided technical expertise to characterize new technologies such as mixed reality trackers in conjunction with its application software.• Proposed and developed an innovative approach to training and introductory equipment for new employees in the mechanical group.• Acted as a change agent to create a career path and personal development grid for employees in the company and expectations for each level.

• Provide a technical advisory role to teams on several aspects of medical product development across the entire division.• Coordinate with the numerous multidisciplinary teams and the Quality, Manufacturing, Maintenance and Regulatory departments.• Act as a resource person to develop and implement new procedures focused on performance and the effectiveness of work methods.• Manage a team of 6 engineers and their distribution to various parallel and active projects according to their expertise and interests.• Maintain cyclical performance metrics and high employee engagement scores.• Coordinate recruitment, training and performance evaluation activities.• Actively participate in cadaveric studies, clinical studies and product validations to demonstrate product performance and reliability.Achievements:• Managed the coordination of a multi-site project with the United States and Europe to develop instrument cases and force sensors for the ROSA® Hip robotic platform product.• Coordinated product development teams with various technologies: 3D printing, new image acquisition and segmentation methods for ankle and jaw reconstruction applications.• Supported workflow improvement with Manufacturing Engineering department to facilitate handoff activities and reduce project timelines by approximately 3 months.• Managed continuous improvement projects from internal and external audits to meet quality system performance metrics.• Proposed a matrix of expertise topics specific to mechanical engineering teams in order to identify resource people and assist employees in their career development.

• Provide a technical advisory role to teams on certain aspects of medical product development across the entire division.• Determine requirements based on initial needs and monitor their evolution throughout the project.• Collaborate with numerous multidisciplinary teams and Quality, Manufacturing and Regulatory departments depending on project activities.• Manage several active group projects in parallel supported by different teams.• Actively participate in cadaveric studies, clinical studies and product validations to demonstrate product performance and reliability.Achievements:• Actively participated in the development of the IAssist® complete knee arthroplasty system which demonstrated optimal surgeon guidance in 95% of cases with 88% good or excellent patient satisfaction.• Acted as Development of the Zimmer® PSI KNEE and Zimmer Biomet® X-PSI™ KNEE single-use systems for total knee arthroplasty, which had the potential to reduce the need for standard instrument trays by 50% and improve costs of hospital procedures.• Acted as point person for the implementation of a local production line and another in the United States to increase production from 100 to 1,250 instruments per month since 2015.

• Concevoir, développer et fabriquer des instruments chirurgicaux selon les besoins du client.• Élaborer des documents de spécifications et des gammes de fabrication d’instruments à usage unique et réutilisables.• Développer des procédés de fabrication compatibles à l’échelle de l’entreprise.• Assister aux opérations de fabrication des produits.Réalisations :• Développé et conçu des outils chirurgicaux pour la chirurgie cardiaque compatible avec les systèmes COR-VASC et COR-VALV.• Participé activement au développement et la commercialisation du produit d’implant Extra-Aortic et les éléments périphériques tels que l’emballage stérile, la poignée d’installation.