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Manufacturing Engineer I

ICONMA, LLC

Plano, TX

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JOB DETAILS
SALARY
$24.67–$27.81 Per Hour
SKILLS
Analysis Skills, Automation, Biotech and Pharmaceutical, Communication Skills, Continuous Improvement, Cross-Functional, Data Analysis, Detail Oriented, ERP (Enterprise Resource Planning), English Language, FDA (Food and Drug Administration), Health Plan, Healthcare, ISO (International Organization for Standardization), Identify Issues, Interpersonal Skills, Lean Manufacturing, Lean Six Sigma, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing Execution Systems (MES), Manufacturing Operations, Manufacturing/Industrial Processes, Medical Equipment, Metrics, Minitab, Operational Support, Operations, Problem Solving Skills, Process Improvement, Process Validation, Production Control, Research & Development (R&D), Root Cause Analysis
LOCATION
Plano, TX
POSTED
3 days ago
Our client, a Medical Device and Healthcare company, is looking for a Manufacturing Engineer I for their Plano, TX location.
 
Responsibilities:
  • The Manufacturing Engineer I supports daily manufacturing operations by troubleshooting production issues, monitoring yield metrics, investigating scrap and defects, and driving continuous improvement initiatives.
  • They will additionally support implementing new equipment and processes using the IQ/OQ/PQ framework.
  • The engineer will work closely with cross-functional teams such as Quality, Production, and R&D at multiple levels to ensure compliant and efficient manufacturing processes.
  • The engineer will independently perform root cause analysis using tools such as 6M and 5 Why and effectively communicate findings to management.
  • Troubleshoot manufacturing and equipment-related issues.
  • Monitor and analyze yield, scrap, and defect data.
  • Drive continuous improvement initiatives.
  • Collaborate with cross-functional teams to ensure smooth operations.
  • Implement and validate new equipment and processes (IQ/OQ/PQ).
  • Document findings and maintain compliance with FDA/ISO standards.
  • Communicate and present status of activities and findings to multiple levels and audiences.
 
Requirements:
  • Excellent or native English language fluency due to all meetings, procedures, and technical communications being in English
  • Evidence of interpersonal, communication, and influence skills with multiple levels of cross functional groups
  • 0–3 years of relevant experience
  • Technical problem-solving
  • Data analysis (yield, scrap, process metrics)
  • Strong communication skills
  • Attention to detail in regulated environments
  • Root cause analysis
  • Internship or co-op in regulated manufacturing (medical devices/pharma)
  • Exposure to Lean Manufacturing or Six Sigma
  • Experience with statistical tools (e.g., Minitab, JMP)
  • Familiarity with ERP or MES systems
  • Hands-on experience with equipment installation or automation
  • Bachelor’s degree in Mechanical Engineering (preferred), Industrial Engineering, Electrical Engineering, Chemical Engineering, or Bioengineering
  • Excellent or native English language fluency due to all meetings, procedures, and technical communications being in English Evidence of interpersonal, communication, and influence skills with multiple levels of cross functional groups looking for an individual who is able to operate independently and drive results in a fast-paced environment.
 
Why Should You Apply?

About the Company

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ICONMA, LLC

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