PneumoWave

📣 WE ARE HIRING 📣 We are currently recruiting for an R&D Test Engineer to support our ongoing development of advanced respiratory monitoring solutions. This role is central to our mission of reducing preventable deaths through real-time, clinically validated digital health technologies. Based at our Eurocentral facility in Scotland, this position offers the opportunity to contribute to a meaningful and technically challenging area of innovation within a collaborative, multidisciplinary team in a hybrid work environment. To learn more about the role, please visit: https://lnkd.in/eVZXaRuc #PneumoWave #TestEngineer #DigitalHealth #MedTech #EngineeringJobs

Thank you, Scottish Development International, for highlighting the role of innovative Scottish companies in tackling global healthcare challenges. We’re proud that PneumoWave’s work in respiratory monitoring is contributing to efforts that support early intervention and prevent avoidable deaths, particularly in the context of opioid-related harm. It's encouraging to see Scotland recognised as a leader in healthtech - driven by collaboration between clinicians, researchers, and industry. We look forward to continuing this important work alongside our peers in the sector.

We’re pleased to share that PneumoWave has received Class II FDA 510(k) clearance for our Data Collection Mobile (DCM) system - a significant regulatory milestone that strengthens our position in the digital health and respiratory care markets. This clearance affirms the depth of our technical, clinical, and regulatory capabilities. Our DCM system - encompassing hardware, software, cybersecurity, usability, and risk management - underwent rigorous FDA scrutiny and was cleared with virtually no objections. This first US clearance is for sleep and activity monitoring with our Biosensor worn on the wrist; it represents a critical step forward in our broader product development strategy and demonstrates strong regulatory confidence in our engineering and ISO 13485 certified quality system. It’s the foundation we need for our chest-worn system that detects breathing trouble in real time. We’re proud of the dedication shown by our engineering, clinical, human factors and regulatory teams in achieving this milestone. It reinforces our trajectory toward scalable, real-time respiratory monitoring solutions with potential global impact. #FDA510k #MedicalDevices #RespiratoryCare #DigitalHealth #PneumoWave #MedTech