Senior Aseptic Packaging Engineer

Kingfisher Recruiting

Indianapolis (IN)

On-site

USD 85,000 - 115,000

Full time

11 days ago

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Job summary

Kingfisher Recruiting represents a world-class client seeking a Manufacturing Engineer in Indiana to lead reliability and packaging improvements in a high-speed production environment.

You will drive data-driven projects, mentor junior engineers, and collaborate with cross-functional teams to reduce cost, increase capacity, and enhance safety and maintenance effectiveness. The role requires 7–10 years of experience and a strong background in FDA/GMP settings and CAD tools.

Qualifications

  • Bachelor’s degree in Engineering required; Mechanical, Chemical or Manufacturing preferred.
  • 7–10 years of engineering experience in a production facility with focus on OEE and process improvements.
  • Hands-on leader with project management experience.
  • Experience in a food-grade FDA/GMP/HACCP environment with high-speed packaging equipment.
  • Strong computer skills with automation and controls knowledge (PLC, DCS).
  • Lean manufacturing and Six Sigma tools experience.
  • Familiar with AutoCad, Inventor, and SolidWorks.

Responsibilities

  • Develop and lead projects focused on reliability and machine efficiency.
  • Perform root cause analysis and drive safety and maintenance improvements.
  • Collect and analyze data to support cost reduction and capacity growth.
  • Teach and train junior engineers and cross-functional teams.

Skills

OEE
Lean manufacturing
Six Sigma
Project leadership
Automation controls

Education

Bachelor’s Degree in Engineering

Tools

AutoCad
Inventor
SolidWorks

Job description

Kingfisher Recruiting represents a world-class client seeking a Manufacturing Engineer in Indiana to lead reliability and packaging improvements in a high-speed production environment.

You will drive data-driven projects, mentor junior engineers, and collaborate with cross-functional teams to reduce cost, increase capacity, and enhance safety and maintenance effectiveness. The role requires 7–10 years of experience and a strong background in FDA/GMP settings and CAD tools.

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