
51 - 200 employees
Founded 2015
🏥 Healthcare
🤖 Artificial Intelligence
🔧 Hardware
🔥 Funding within the last year
💰 $29.4M Venture Round - Sunrise on 2025-09
Healthcare • Artificial Intelligence • Hardware
Sunrise is a medical device company that provides a single‑sensor home sleep apnea test using mandibular jaw movement (MJM) bio-signals to diagnose obstructive sleep apnea and related sleep-disordered breathing. Their 8‑gram wearable sensor, paired with an AI‑scored reporting platform and a healthcare professional portal, delivers rapid, clinically validated results for use by clinicians; the technology has FDA De Novo clearance, NICE recommendation for home diagnosis, and multiple peer‑reviewed validations against polysomnography.
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51 - 200 employees
Founded 2015
🏥 Healthcare
🤖 Artificial Intelligence
🔧 Hardware
🔥 Funding within the last year
💰 $29.4M Venture Round - Sunrise on 2025-09
Healthcare • Artificial Intelligence • Hardware
Sunrise is a medical device company that provides a single‑sensor home sleep apnea test using mandibular jaw movement (MJM) bio-signals to diagnose obstructive sleep apnea and related sleep-disordered breathing. Their 8‑gram wearable sensor, paired with an AI‑scored reporting platform and a healthcare professional portal, delivers rapid, clinically validated results for use by clinicians; the technology has FDA De Novo clearance, NICE recommendation for home diagnosis, and multiple peer‑reviewed validations against polysomnography.
• Establish and control the flow of materials, components and finished devices across manufacturing and clinic operations • Plan inventory and optimize stock levels, carrying costs and storage costs • Select and implement inventory management tooling and reporting cadence • Define and own inventory KPIs • Build and maintain the master production/supply plan with the manufacturing team • Identify and escalate supply risks and maintain dual-sourcing or contingency plans • Coordinate kitting, fulfillment and returns for HST devices, PAP machines and accessories • Manage international logistics for customer orders across the EU, UK, US and Australia • Own landed shipping costs, evaluate carriers and freight forwarders, and renegotiate terms • Manage Incoterms, customs classification, denied-party/export screening and other trade-compliance obligations • Model and reduce customs/duties exposure on EU-manufactured devices entering the US • Report shipping cost per device/shipment to the executive team • Manage US 3PL relationships, contracts, SLAs, performance reviews, RFPs and escalations • Manage the operational interface between 3PLs and internal systems, including order flow, inventory synchronization and returns processing • Negotiate and manage procurement contracts for raw materials, components and clinic finished goods • Manage vendor selection, pricing negotiations and supplier contract terms • Maintain supplier performance scorecards and drive renewal/renegotiation cycles • Execute supplier qualification, approved supplier list maintenance and quality agreements with Quality/Regulatory • Own lot/UDI traceability from raw materials through finished devices and shipped units • Document procurement and logistics activities for inspection and audit readiness • Coordinate with Manufacturing, Quality/Regulatory, Finance, Dreem Health clinical operations, Customer/Patient Care, freight forwarders, customs brokers, 3PLs and hardware suppliers
• 5+ years in supply chain, logistics, or operations management, including direct ownership of inventory planning and carrier/3PL relationships • Demonstrated track record of reducing shipping/logistics cost at a company shipping physical goods internationally, ideally EU↔US • Experience managing 3PL relationships in the US: contracting, SLA management, performance review • Working knowledge of import/customs processes for goods moving from the EU into the international (US, UK, AU) • Hands-on experience with an ERP/MRP system (demand planning, inventory, production scheduling modules) as a super-user or functional owner, not just an end user • Comfort building process and tooling from a low-maturity baseline rather than optimizing an existing mature system • Full professional fluency in English • Experience in a regulated manufacturing environment (medical device, pharma, or similarly regulated hardware) with working knowledge of ISO 13485, EU MDR, and/or cGMP as applied to supply chain and procurement • Direct procurement/purchase-contract negotiation experience with hardware manufacturers or raw material suppliers • Experience with reverse logistics / return programs • French language skills are preferred
• Remote/hybrid work in the EU • Periodic US travel for 3PL site visits, vendor negotiations and carrier reviews (at minimum once a year)
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