Principal Polymer Processing Engineer - Remote

CONMED Corporation

Largo (FL)

Remote

USD 139,000 - 177,000

Full time

8 days ago

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Benefits offered by this job

Competitive compensation
Excellent healthcare
401K with company match
Tuition assistance
Employee referral program

Job summary

CONMED Corporation is seeking a Principal Polymer Processing Engineer - Injection Molding in Largo, FL. This role leads technical initiatives across design, tooling, process development, and validation for medical device components.

You will partner with R&D, Manufacturing, Quality, Regulatory and Supply Chain to drive product transfers, process optimization, and manufacturing readiness while maintaining compliance with FDA quality systems.

Qualifications

  • Bachelor’s degree in Polymer/Plastics/related engineering required.
  • 10+ years of progressively responsible engineering experience in injection molding/polymer processing.
  • Experience troubleshooting injection molded parts and steering root-cause analysis across design, material, process and tooling.

Responsibilities

  • Provide technical leadership for complex injection molding processes, molds, and supporting technologies.
  • Lead development, qualification and validation of molding processes and equipment.
  • Define processing windows and control strategies to ensure repeatable manufacturing.
  • Mentor engineers and collaborate across functions to meet product, quality and cost goals.
  • Support manufacturing transfers, repairs, and process improvements across sites.

Skills

Injection molding
Polymer processing
Mold design
Process validation
Statistical analysis
Troubleshooting
Technical leadership
Cross-functional collaboration

Education

Bachelor's degree in Polymer/Plastics/related Eng
Master's degree in Polymer/Plastics/Materials (preferred)

Tools

Mold-flow analysis tools
Mold-flow simulation

Job description

CONMED Corporation is seeking a Principal Polymer Processing Engineer - Injection Molding in Largo, FL. This role leads technical initiatives across design, tooling, process development, and validation for medical device components.

You will partner with R&D, Manufacturing, Quality, Regulatory and Supply Chain to drive product transfers, process optimization, and manufacturing readiness while maintaining compliance with FDA quality systems.

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