Senior Manufacturing Engineer

Stryker

Fort Lauderdale (FL)

On-site

USD 78,000 - 130,000

Full time

3 days ago
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Job summary

Stryker Robotics in Fort Lauderdale, FL is seeking a Manufacturing Engineer to support the assembly of complex electromechanical systems on the production floor. You will work with cross-functional teams to drive quality, throughput, and cost improvements.

This role emphasizes hands-on problem solving, data analysis, and adherence to FDA/ISO quality systems in a regulated manufacturing setting. You will perform IQ/OQ/PQ, develop work instructions, and help introduce new products with robust

Qualifications

  • Must have a Bachelor's degree in an engineering discipline such as Mechanical, Industrial, Biomedical, Electrical, Manufacturing, or Robotics.
  • Minimum 2 years of manufacturing engineering experience.
  • Experience with regulated manufacturing environments.
  • Experience in complex mechanical/electromechanical assemblies.

Responsibilities

  • Provide direct manufacturing engineering support to production operations and troubleshoot process issues.
  • Lead root-cause investigations and drive timely corrective actions.
  • Execute IQ/OQ/PQ and equipment qualification activities per quality system.
  • Analyze manufacturing data to improve process capability and cost performance.
  • Collaborate with Quality, R&D, and Supply Chain on manufacturability and new product introductions.
  • Develop and maintain manufacturing documentation including SOPs and control plans.

Skills

Root cause investigations
Statistical analysis
Process improvement
Cross-functional collaboration

Education

Bachelor’s degree in Mechanical Engineering
Bachelor’s degree in Industrial Engineering
Bachelor’s degree in Biomedical Engineering
Bachelor’s degree in Electrical Engineering
Bachelor’s degree in Manufacturing Engineering
Bachelor’s degree in Robotics Engineering

Tools

SolidWorks
Minitab
GD&T

Job description

At Stryker Robotics, manufacturing engineering plays a critical role in delivering reliable, high-quality robotic systems that support healthcare providers around the world. In this role, you will partner across engineering, quality, operations, and supply chain teams to improve manufacturing performance, support new product introductions, and drive operational excellence on the production floor.

This position provides hands‑on manufacturing engineering support for the assembly of complex electromechanical systems while leveraging data, process improvements, and problem‑solving methodologies to enhance quality, efficiency, throughput, and cost performance.

What You Will Do
  • Provide direct manufacturing engineering support to production operations by troubleshooting process issues, leading root cause investigations, and driving timely resolution of manufacturing challenges.
  • Execute manufacturing process validation and equipment qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), in compliance with quality and regulatory requirements.
  • Analyze manufacturing data using statistical tools to improve process capability, support measurement system analysis, and identify opportunities to improve quality, throughput, ergonomics, and cost.
  • Collaborate with Quality, Research & Development, Advanced Operations, and Supply Chain teams to support design for manufacturability, new product introductions, production readiness activities, and continuous improvement initiatives.
  • Develop and maintain manufacturing documentation, including work instructions, standard operating procedures, process failure mode and effects analyses, control plans, and visual aids in accordance with quality management system requirements.
What You Will Need
Required:
  • Bachelor’s degree in Mechanical Engineering, Industrial Engineering, Biomedical Engineering, Electrical Engineering, Manufacturing Engineering, Robotics Engineering, or a related engineering discipline.
  • Minimum 2 years of manufacturing engineering experience.
  • Experience supporting complex mechanical and/or electromechanical assemblies.
  • Experience working within a regulated manufacturing environment.
Preferred:
  • Experience in medical device, robotics, high-tech assembly, or other regulated manufacturing industries.
  • Experience supporting nonconformance investigations, corrective and preventive actions, process validation, and continuous improvement initiatives.
  • Knowledge of FDA Quality System Regulations, ISO 13485, ISO 14971, and risk‑based validation methodologies.
  • Proficiency with engineering and statistical analysis tools such as SolidWorks, Minitab, and Geometric Dimensioning & Tolerancing (GD&T).
United States of America Pay Ranges:

$77,700 - $129,500 USD Annual

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