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Manufacturing Sr Engineer I
Manufacturing Sr Engineer I-May 2024
Indianapolis
May 28, 2026
About Manufacturing Sr Engineer I

  At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

  As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.

  What You Can Expect

  The Manufacturing Senior Engineer I is responsible for:

  • Creating, maintaining, and improving controlled technical documents such as prints, procedures, bill of materials and routers.

  • Supporting a wide variety of processing applications such as, but not limited to, machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc.

  • Establishing and improving process methods which meet performance and quality requirements.

  • Developing and executing project plans and schedules for work activities.

  • Communicate (written and verbal) direction and project plans with appropriate personnel from other departments.

  • Evaluating multiple options to select the most appropriate processes and machining methods.

  • Execute tasks related to equipment qualification and/ or process validation project(s).

  Your Background

  Requires a Bachelor's degree in mechanical engineering, industrial engineering or related field.

  Must have 3 years of experience in the position offered or related position.

  Must have:

  3 years of experience with FDA regulated medical device industry regulations with regards to Quality control procedures and systems, such as Engineering ChangeManagement System, Nonconformance Report and Disposition, Engineering Specifications, problem solving with root cause analysis, and Work Instructions.

  3 years of experience executing tasks related to equipment qualification.

  1 year of experience executing CNC functional testing.

  1 year of experience analyzing and troubleshooting equipment related to validated cleaning processes.

  3 years of experience developing and executing project plans and task scheduling.

  3 years of experience with statistical analysis, process development and geometric dimensioning & tolerancing.

  Travel Expectations

  Role requires up to 10% foreign/domestic travel.

  EOE/M/F/Vet/Disability

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