Senior Product Manager

Overview

At Spacelabs Healthcare, we are on a mission to p rovide continuous innovation in healthcare technology for better clinical and economic outcomes. Our scalable solutions deliver critical patient data across local and remote systems, enable better-informed decisions, increase efficiencies, and create a safer environment for patients.

Why work at Spacelabs? Because lives depend on you!

Role Overview

We are seeking a strategic and experiencedSenior Product Managerto lead the development and lifecycle management of ourdiagnostic cardiology portfolio, with a strong focus on ournext-generation cloud-based workflow and analysis platform. This role is critical in shaping the future of our Diagnostic Cardiology division by integrating cutting-edge technology with clinical insights to deliver impactful solutions. The ideal candidate will bring deep domain expertise inHolter monitoring, ambulatory blood pressure monitoring, EKG carts, or related cardiac diagnostics, and a proven track record inSoftware as a Medical Device (SaMD)andcloud-based software platforms.

Responsibilities

• Define and drive the product vision, roadmap, and strategy for the diagnostic cardiology portfolio.
• Translate market trends, customer needs, and clinical requirements into innovative product solutions.
• Lead cross-functional teams through the product development lifecycle, from concept through launch and post-market support.
• Collaborate with engineering, clinical, regulatory, and commercial teams to ensure timely and compliant product delivery.
• Engage with key opinion leaders, clinicians, and customers to gather insights and validate product direction.
• Represent the voice of the customer in all product decisions.
• Drive the development and optimization of cloud-based workflow and analysis tools, ensuring scalability, security, and compliance.
• Partner with software engineering teams to deliver intuitive, high-performance user experiences.
• Ensure all products meet regulatory requirements for SaMD, including FDA, CE, and other global standards.
• Support documentation and submission processes as needed.

Qualifications

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