# Sr. Systems Engineer (New Kensington, PA) at Philips

Philips is hiring a Sr. Systems Engineer (New Kensington, PA). It pays $127k-$202k a year and Level rates it Little AI ●○○○; you can [apply on Philips](https://jobsbylevel.com/go/bd46ad6a-e06b-4436-9ce5-1568f4c25abd?utm_medium=ai-agent).

AI Level 1, AI centrality 32 out of 100. New Kensington, Pennsylvania, United States.

## Details

- Company: [Philips](https://jobsbylevel.com/companies/philips)
- AI level: AI Level 1 (score 32 out of 100)
- Location: New Kensington, Pennsylvania, United States
- Salary: $127k-$202k
- Posted: November 12, 2026
- Apply: https://jobsbylevel.com/go/bd46ad6a-e06b-4436-9ce5-1568f4c25abd?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=sr-systems-engineer-new-kensington-pa-at-philips-10d851

## Description

Job Title Sr. Systems Engineer (New Kensington, PA) Job Description Sr. Systems Engineer – Sleep & Respiratory Care The Senior Systems Engineer will play a critical role as a part of the Sleep and Respiratory Care R&D/Systems Engineering Team that is responsible for developing and sustaining respiratory ventilators and sleep therapy devices, ensuring our Sleep & Respiratory Care (S&RC) products are safe, reliable and of the highest quality. Your role: Responsible for the overall Systems Engineering deliverables and activities including translation of user and business requirements to product requirements, technical approach and system architecture development, harmonization of system design among the relevant products and projects of the segment(s), allocation of derived requirements to subsystems, and integration strategy and methods. Drives refinement and translation of user requirements (including but not limited to clinical, serviceability, reliability, and manufacturability), regulatory requirements, and system architecture and concepts into functional requirements. Manage requirements to be compliant with requirement management policies and ensure coverage, quality, and full implementation of requirements. Responsible for technical approach, system top level design, feasibility of potential technical solutions, and allocation of derived requirements (including functionality, interface specifications and design budgets) onto affected subsystems. Plans and executes system-level design reviews. Owns system-level defect analysis and remediation during System Integration, Verification and Validation phases. Supports Product Risk Management, regulatory and standard fulfillment and country approval. Manages technical risk by conducting thorough risk analyses, including Design Failure Mode and Effects Analysis (DFMEA), and developing risk control measures. May require travel up to 10%. You're the right fit if: You’ve acquired 7+ years of experience successfully developing complex medical devices and a focus in systems engineering (hardware, software, consumables), with experience in Sleep Therapy/Ventilation products and accessories highly desired. Your skills include: A strong understanding of the System Design process, including Model-Based (MBSE/V-Model) Design approach-conceptualization, writing requirements, functional and technical design, check & optimize, verification, integration and finally validation. Experience in test-driven design methodologies, analytical and architectural thinking, system view, physical insight, flexibility, and a hands-on mentality to deliver sustainable results and creative solutions. Strong knowledge of Medical Device/ FDA Quality System Regulations (ISO 13485/14971/10993/18562 ,17510 2015, IEC 62366 etc.) and clearance processes. You have a Bachelor’s Degree in Engineering- Systems, Biomedical, Mechanical or similar discipline (required). Master’s degree (preferred). You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this position . You have effective communication, computer, documentation, presentation, and interpersonal skills, as well as the ability to work independently, cross-functionally, and collaboratively. You’ve demonstrated a relentless focus on Patient Safety and Quality as an organizational value. How we work together We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an office role. About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we

The description is cut here. Read the full offer: https://jobsbylevel.com/jobs/sr-systems-engineer-new-kensington-pa-at-philips-10d851

Source: https://jobsbylevel.com/jobs/sr-systems-engineer-new-kensington-pa-at-philips-10d851

## Cite this page

Level. https://jobsbylevel.com/jobs/sr-systems-engineer-new-kensington-pa-at-philips-10d851.

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