Project manager r&d_medical devices

10 ago - Italia
IT10656-ALMS Air Liquide Medical Systems

Air Liquide Medical Systems srl, part of the Air Liquide Group, is the business line of the Air Liquide Healthcare Division dedicated to Medical Devices. The company develops, manufactures and sells innovative products for the treatment of respiratory diseases. Ventilation: ventilators and patient interface devices (masks) for intensive care, emergency treatments, transport treatments and home therapy. Aereosoltherapy devices Devices for the emanation of medical gases We are looking for an engineer with product development and project management skills to join an R&D; team in a medical devices company focused on innovations. You'll be part of a primary international company as a member of our young and dynamic engineering team and you will contribute to the design of cutting‐edge products. Responsibilities Improve the product development process by reducing time‐to‐market and driving efficiency to shorten product development timelines. Translate market insights and user needs into comprehensive technical specifications and product roadmaps.



Lead the definition of patient‐centric product requirements to enhance ergonomics, comfort and clinical efficacy. Execute detailed techno‐economic feasibility analyses to ensure product viability and strategic alignment with organizational objectives. Contribute to the company's IP portfolio through the generation of patentable engineering solutions. Successfully reduce production costs by implementing strategic DTC methodologies without compromising medical‐grade quality. Ensure compliance with the company's safety and environmental standards. Manage the relationship with suppliers to realize prototypes using the most recent additive manufacturing technologies. Analyze prototypes, collect data and conduct tests as needed. Manage documentation of both new and revised 3 D designs, write detailed reports and prepare quality control checklists. Develop technical documentation according to Medical Devices EU regulations to grant CE ce

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