Mechanical Engineer

Siemens Healthineers

Mechanical Engineer developing complex medical-device subsystems for Siemens Healthineers. Leading design, verification, validation, and production release across multidisciplinary teams.

Posted 8/19/2026full-timeTarrytown • New York • 🇺🇸 United StatesSeniorLead💰 $128,480 - $176,660 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in mechanical and electro-mechanical subsystem design, with a strong focus on product development in FDA-regulated environments. Proficient in utilizing advanced CAD software and leading engineering analysis, verification testing, and compliance documentation.

Highest-signal resume keywords

Mechanical Engineering Degree8+ Years Product Design ExperienceAdvanced Siemens NX ProficiencyFDA Design Controls ExperienceStrong GD&T Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Mechanical DesignElectromechanical DesignEngineering AnalysisTolerance Stack-UpsGD&T Best PracticesFMEADFMAFEA SimulationCFD SimulationReliability Engineering

Soft Skills

Excellent Communication SkillsMentoring Engineers

Tools & Technologies

NX 3D CAD SoftwareTeamcenter PLMISO 14971 Risk ManagementLean Six SigmaAgile Methodologies

Certifications & Qualifications

PMP Certification

Industry Keywords

FDA-Regulated EnvironmentsClass II Medical DevicesClass III Medical DevicesIEC StandardsGlobal Manufacturing Support

Tech Stack

Tools & technologies

PMP

About the role

Key responsibilities & impact

Lead design and development of complex mechanical and electro-mechanical subsystems
Drive product development activities from concept, prototyping, verification, validation, and production release
Perform engineering analysis, tolerance stack-ups, and design reviews
Create and approve engineering drawings utilizing GD&T best practices
Lead root cause investigations and corrective actions
Partner with suppliers, manufacturing, quality, regulatory, and service teams
Execute verification testing and document results for regulatory compliance
Serve as a subject matter expert and mentor junior engineers

Requirements

What you’ll need

Bachelor's Degree in Mechanical Engineering
8+ years of product design and development experience
Experience in FDA-regulated environments
Advanced proficiency with NX or comparable 3D CAD software
Experience with Teamcenter or similar PLM systems
Strong GD&T, FMEA, DFMA, and manufacturing knowledge
Strong electromechanical design experience
Excellent communication skills
Master's Degree in Mechanical, Biomedical, or Mechatronics Engineering preferred
Experience developing Class II or Class III medical devices preferred
Experience leading products through the full development lifecycle preferred
Advanced Siemens NX and Teamcenter expertise preferred
Hands-on FEA and CFD simulation experience preferred
Knowledge of ISO 14971 risk management methodologies preferred
Experience with FDA Design Controls and IEC standards preferred
Expertise with motors, drives, sensors, actuators, and motion control systems preferred
Knowledge of reliability engineering and accelerated life testing preferred
Experience supporting global manufacturing and supplier qualification preferred
Lean Six Sigma, Agile, or PMP certifications are a plus
Experience mentoring engineers and leading technical reviews preferred
Successful candidate must be able to work with controlled technology in accordance with US export control law

Benefits

Comp & perks

medical insurance
dental insurance
vision insurance
401(k) retirement plan
life insurance
long-term and short-term disability insurance
paid parking/public transportation
paid time off
paid sick and safe time