Full-Time
Software Technologist
Mobile
Posted on 9/23/2025
Philips
Manufactures sleep therapy and respiratory devices
No salary listed
Bengaluru, Karnataka, India
In Person
Office-based role requiring in-person presence at least 3 days per week.
 Software Engineering (1) |
|---|
- At least a Bachelor’s degree in Engineering, Computer Science or equivalent work experience
- 5-9 years of experience working as a Software engineer in mobile platforms
- Excellent designing, coding and debugging skills
- Hands-on mobile application architecture design and development in android and/or iOS platform using technologies like React Native - React native, React, TypeScript, JavaScript(must have), Android – Java, Kotlin, Gradle, iOS – Objective C, Swift, Database – SQLite, Realm
- Object oriented design
- Generic Database design skills
- Unit test frameworks like MS unit test or Nunit
- Experience with software design concepts, practices, modern development methodologies such as Clean Code and CI/CD pipelines on Git
- Agile development planning, story points estimation
- Collaboration and working in MS Teams and SharePoint
- Problem solving and analytical skills to troubleshoot and understand current product
- Working with Cross geographical team
- Mentor Junior engineers.
- Participates in full software development processes, working with broader autonomy and in pairing mode with other software team members, challenging requirements, design, and quality.
- Serves as a recognized technical expert in specific areas within the team, leading the creation of software designs and providing guidance on best practices.
- Takes on moderately complex software development tasks, collaborating with senior team members to deliver high-quality software solutions that meet project requirements.
- Develops and executes comprehensive test plans, including unit, integration, and system tests, to ensure software reliability, performance, and adherence to specifications.
- Conducts thorough code reviews to ensure adherence to coding standards, identify potential bugs, and promote best practices in software development, fostering a culture of continuous improvement and high-quality code.
- Supports DevOps in deploying software, setting, monitoring, and ensuring own performance metrics are met, while also defining, monitoring, and meeting broader performance and quality metrics.
- Diagnoses and resolves software defects by analyzing logs, reproducing issues, and implementing effective fixes to enhance software reliability and performance.
- Creates and maintains comprehensive technical documentation, including system architecture diagrams, API specifications, and user guides to facilitate knowledge sharing and support.
- Keeps abreast of emerging technologies, industry trends, and best practices in software development to continuously improve skill sets and apply innovative solutions.
- Applies analytical skills to resolve medium complexity requests efficiently, exercising judgment within defined procedures/practices to determine appropriate action.
- Medical devices and standards like FHIR/HL7 knowledge is a plus
- Highly regulated industry experience
- Agile and traditional frameworks for software development
- SAFE certification is a plus
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.
Help us improve and share your feedback! Did you find this helpful?
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.
Register now for your free virtual pass to the Low-Code/No-Code Summit this November 9. Hear from executives from Service Now, Credit Karma, Stitch Fix, Appian, and more. Learn more. Philips Norelco is creating an interactive metaverse experience called Shavetopia in Roblox, based around the Movember trend. For anyone who doesn’t know what that is, Movember is where people grow facial hair for the entire month of November. The portmanteau comes from adding the word mustache to the name of the month