Medical Devices Systems Engineer – Sleep & Respiratory Care

Philips; New Kensington (Westmoreland County); On-site; USD 102,000 - 163,000; Full time

Benefits offered by this job

PTO

401(k) match

HSA with company contribution

Stock purchase plan

Education reimbursement

Job summary

Philips is seeking a Systems Engineer in New Kensington, PA to lead system-level design for Sleep and Respiratory Care devices. You will translate user and regulatory requirements into product specifications, drive architecture development, and coordinate subsystem integration across projects.

Ideal candidates have 2+ years in medical devices with MBSE experience, strong emphasis on patient safety, and familiarity with FDA/ISO quality systems.

Qualifications

• 2+ years of experience developing complex medical devices with a focus in systems engineering (hardware, software, consumables).
• Experience in Sleep Therapy/Ventilation products and accessories is highly desired.
• Bachelor’s degree in Engineering required; Master’s degree preferred.

Responsibilities

• Owns system-level deliverables and translates user/business requirements into product requirements and architecture.
• Leads refinement and translation of requirements to functional specs; ensures coverage and traceability.
• Plans and executes system-level design reviews and allocates requirements to subsystems.
• Manages system integration, verification, and validation with defect analysis and risk management.
• Conducts DFMEA and supports regulatory and country approvals.

Skills

MBSE

Requirements engineering

System architecture

Regulatory compliance

Cross-functional collaboration

Education

Bachelor’s Degree in Engineering

Master’s degree preferred

Tools

DFMEA

Job description

Philips is seeking a Systems Engineer in New Kensington, PA to lead system-level design for Sleep and Respiratory Care devices. You will translate user and regulatory requirements into product specifications, drive architecture development, and coordinate subsystem integration across projects.

Ideal candidates have 2+ years in medical devices with MBSE experience, strong emphasis on patient safety, and familiarity with FDA/ISO quality systems.