Full-Time
Senior Software Technologist-Embedded
Linux Kernel, Board Support Package and Yocto
Posted on 5/7/2026
Philips
Manufactures sleep therapy and respiratory devices
No salary listed
Bengaluru, Karnataka, India
Hybrid
Three days on-site per week required.
 Software Engineering (1) |
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- 8+ years of relevant experience as a developer working in a Linux development environment
- At least 6+ years of experience in developing Custom Embedded Linux Operating Systems using Yocto, BitBake recipes and OpenEmbedded
- Experience in embedded development, Linux device driver development, integration, board bring-up activities such as programming, debugging, troubleshooting and functionality testing
- Advanced knowledge of C, C++, shell scripts, Python and proven hands-on experience
- Good understanding in electronics hardware: schematics, data sheets reading
- Solid knowledge of Embedded Linux systems, low-level software (drivers, BSP), open-source, Yocto, and proven hands-on experience
- Modify/patch or rewrite device tree files, bootloaders, kernel drivers, or open-source packages with a clean commit & potentially contribute back to OSS community
- Sound knowledge of GNU/Yocto build system as well as using various tool chains
- Proficiency in GitHub, CI/CD pipelines, and Agile/SAFe methodologies
- Excellent problem-solving, analytical, and debugging skills
- Strong communication, documentation, and collaboration skills
- Work experience in healthcare systems or real-time applications
- Basic understanding of medical technology & human physiology (preferred)
- Analyze and understand software/functional requirements to design and develop high-quality software.
- Lead architecture decisions and ensure scalable, high-performance solutions.
- Write efficient, maintainable code following best practices and conduct code reviews.
- Developing Bare Metal and/or Linux drivers for Embedded devices based on iMX processors.
- Developing or customizing board support packages (BSP).
- Implement developer-level testing (unit, component) to ensure software reliability.
- Writing component tests using Google Test (GTest) with Gherkin syntax following behavior-driven development (BDD) principles.
- Create technical documentation and comply with development policies.
- Debug, troubleshoot, and resolve complex software issues efficiently.
- Stay updated with technical advancements and advocate best practices within the team.
- Support project estimation, planning, and risk management activities
- Basic understanding of medical technology & human physiology (preferred)
Philips Respironics designs sleep and respiratory care devices, including CPAP and BiPAP machines, ventilators, and oxygen concentrators, plus related systems. These devices deliver regulated air pressure, support or assist breathing, and provide concentrated oxygen, often paired with software and data tools for monitoring. The division differentiates itself through its long history within Philips and its integrated ecosystem that connects devices with analytics and clinical support across hospital, clinic, and home settings. Its goal is to improve quality of life and clinical outcomes for people with sleep and respiratory conditions by offering reliable devices, patient support, and data-driven care.
Company Size
N/A
Company Stage
Acquired
Total Funding
$5.1B
Headquarters
Murrysville, Pennsylvania
Founded
1891
Simplify's Take
What believers are saying
- BioTelemetry acquisition in 2020 expands remote heart monitoring.
- $479 million settlement in September 2023 closes US litigation.
- New silicone foam validated safe, enabling global device sales.
What critics are saying
- ResMed seizes US sleep market share within 6-12 months.
- FDA consent decree blocks US sales until after 2026.
- January 2024 US ventilation exit halves revenue permanently.
What makes Philips unique
- Pioneered CPAP therapy as standard for sleep apnea since 1976.
- Leads in non-invasive ventilation and home respiratory support.
- Integrates devices with software for data-driven clinical outcomes.
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Benefits
Health Insurance
401(k) Retirement Plan
401(k) Company Match
Unlimited Paid Time Off
Health Savings Account/Flexible Spending Account
Company News
<img src="https://hitconsultant.net/wp-content/uploads/2024/04/Philips.webp" alt="Philips Respironics Reaches Final Agreement with US Regulators on Sleep Apnea Device Recall. " class="wp-image-78777" srcset="https://hitconsultant.net/wp-content/uploads/2024/04/Philips.webp 700w, https://hitconsultant.net/wp-content/uploads/2024/04/Philips-300x161.webp 300w, https://hitconsultant.net/wp-content/uploads/2024/04/Philips-290x155.webp 290w" sizes="(max-width: 700px) 100vw, 700px">What You Should Know: – Philips Respironics, a subsidiary of Royal Philips, has finalized a consent decree with the US Department of Justice (DOJ) and Food and Drug Administration (FDA) to address issues raised during a 2021 inspection of a Philips facility in Pennsylvania.– The agreement focuses on Philips Respironics’ operations in the US, particularly regarding the recall of certain sleep and respiratory care devices.– The company’s focus will now be on completing remediation efforts, ensuring patient safety, and regaining regulatory approval to resume sales of new devices in the US.Focus on Remediation and ComplianceThe consent decree outlines a roadmap for Philips Respironics to:Prioritize Recall Remediation: Philips will continue efforts to remediate millions of sleep apnea and respiratory care devices recalled in June 2021 due to potential health risks associated with degraded sound abatement foam.Independent Oversight: Independent experts will be brought in to review recall remediation efforts and ensure Philips Respironics’ business operations comply with FDA regulations.Continued Patient Support: Philips Respironics can continue servicing existing devices in the hands of patients and healthcare providers. Additionally, they can sell accessories, consumables, and replacement parts for these devices.Sales Restrictions Remain in USThe FDA has not yet authorized Philips Respironics to resume sales of new CPAP, BiPAP, or other respiratory care devices in the US. This restriction will remain in place until Philips meets the requirements outlined in the consent decree.Global Sales Continue with RestrictionsPhilips Respironics can continue to sell new devices, accessories, consumables, and replacement parts outside the US, subject to specific requirements.Safety of Devices with New Foam ConfirmedPhilips Respironics has conducted tests on devices using a new silicone sound abatement foam and found no safety issues. Patients can continue to use these devices following the instructions for use.Financial ImpactPhilips anticipates incurring costs associated with remediation activities and profit disgorgement related to US sales. These costs are estimated at 100 basis points in 2024. The company’s previously announced 2023-2025 financial outlook remains unchanged, already factoring in the consent decree. “Strengthening patient safety and quality remains Philips’ highest priority and the increased scrutiny will help us to improve even more
Following a recall of millions of its breathing machines that began in mid-2021, Phillips Respironics announced Monday that it would halt sales of all such machines within the United States.
In June of 2021, Philips began a recall of over five million of its breathing devices due to toxic fume and substances emanating from the devices’ sound abatement foam.
February 2019 – Koninklijke Philips launched the EPIQ Elite ultrasound system in the market.
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