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Spacelabs Healthcare

Spacelabs Healthcare

www.spacelabshealthcare.com

2 Jobs

804 Employees

About the Company

Founded in 1958, Spacelabs developed the first vital signs monitoring for NASA astronauts culminating in Neil Armstrong wearing Spacelabs telemetry for the moon landing in 1969. Today our patient monitoring and diagnostic cardiology solutions help healthcare organizations around the world maximize care team performance to achieve their own missions.

Spacelabs delivers 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.

Renowned for its open architecture interfacing, Spacelabs is able to connect to a host of hospital data management systems enabling easy flow and review of patient data. Our goal is to provide innovative tools and solutions to aid and accelerate the clinician’s decision making process.

Listed Jobs

Company background Company brand
Company Name
Spacelabs Healthcare
Job Title
Senior Cybersecurity Manager
Job Description
**Job title** Senior Cybersecurity Manager **Role Summary** Lead the cybersecurity and privacy posture for cloud‑based products, driving integration of Privacy & Security by Design across the product lifecycle. Act as product owner for cyber security, manage a dedicated cybersecurity team, and collaborate with product, engineering, quality, and regulatory groups to ensure confidentiality, integrity, and availability of solutions. **Expactations** - Deliver a secure product portfolio that meets medical device and healthcare regulatory requirements. - Drive continuous risk management, incident response, and compliance readiness. - Provide clear security leadership and mentorship to cross‑functional teams. **Key Responsibilities** - Lead and mentor a cybersecurity team, assigning tasks and monitoring progress. - Own the product‑level cybersecurity strategy: threat modeling, secure design, secure SDLC, and security testing. - Advocate for security and privacy throughout product development, ensuring compliance with FDA, HIPAA, GDPR, ISO 27000 series, ISO 13485, ISO 14971, and related standards. - Conduct risk assessments, manage vulnerability reports, and oversee incident investigations. - Develop and maintain product security documentation: labeling, security statements, and compliance evidence. - Collaborate with engineering, quality, and regulatory teams to embed security controls by design and by default. - Provide security guidance to stakeholders, clients, and auditors. **Required Skills** - 10+ years of cybersecurity engineering with 5–10 years of cloud security experience (AWS preferred). - 5+ years leading product cybersecurity projects and risk management in medical device or healthcare domain. - Deep knowledge of secure SDLC, cloud architecture, and security controls (IAM, network, OS, database, web). - Expertise in regulatory frameworks: FDA Cybersecurity Guidelines, 21 CFR 820, ISO 27001/27017/27018, ISO 13485, ISO 14971, EU‑GDPR, HIPAA, AAMI TIR 57, SB 1386. - Strong understanding of Windows/Linux hardening, network security, and cloud best practices. - Proven ability to deliver security solutions that meet industry standards and certifications. - Excellent communication, stakeholder management, and leadership skills. **Required Education & Certifications** - Bachelor’s degree in Computer Science, Information Security, Cybersecurity, or Software Engineering with ≥15 years of related experience *or* Master’s degree with ≥10 years of related experience. - Professional certifications: CISSP, CISM, CISA, Security+, Cloud Security Alliance (CSA), or SANS Cloud Security. ---
Edinburgh, United kingdom
Hybrid
Senior
13-01-2026
Company background Company brand
Company Name
Spacelabs Healthcare
Job Title
Senior Software Engineer
Job Description
**Job Title** Senior Software Engineer **Role Summary** Lead the design, development, and delivery of embedded software for patient monitoring and connectivity systems. Own architecture, code quality, and cybersecurity considerations while collaborating with cross‑functional teams in an Agile environment. Demonstrate technical leadership, mentor peers, and uphold rigorous software engineering practices under regulated medical device standards. **Expectations** - Deliver robust, secure, and compliant software on schedule. - Maintain high coding, testing, and documentation standards. - Advocate for functional, performance, and safety requirements in product design. - Foster collaborative relationships with engineering, QA, regulatory, and international teams. **Key Responsibilities** - Define and validate requirements for patient monitoring products. - Participate in architecture, software design, interface, and UI reviews. - Design, implement, debug, document, and release components for communication, storage, and analysis of physiological data. - Produce design documentation, unit tests, and other artifacts required for compliance. - Mentor junior engineers, ensuring adherence to company values and ethical standards. - Work within a regulated development environment, applying Design Control (21 CFR 820), ISO 14971, and IEC 62304 where applicable. **Required Skills** - 8+ years of professional software engineering experience. - 4+ years of C++11+ OOP development and multi‑threading proficiency. - Embedded Linux application development experience. - Desktop UI experience (Qt/QML, WPF, WinUI 3, UWP) – not WinForms/Win32/web. - Knowledge of ISO 14971, IEC 62304, and 21 CFR 820 (medical device compliance). - Experience with regulated environments (medical, defense, finance, aerospace). - Familiarity with containers, DevOps, continuous delivery, and Agile methodologies. - Proficiency with Git‑based workflows and Azure DevOps (or similar). - Ability to work effectively with international teams (Europe, India, U.S.). **Required Education & Certifications** - Bachelor of Science in Computer Engineering, Computer Science, Mathematics, or a related engineering discipline. - Applicable certifications in medical device software or regulated development (e.g., ISO 14971, IEC 62304) are a plus.
Edinburgh, United kingdom
On site
Senior
18-01-2026