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Quality Sr Engineer I
Quality Sr Engineer IZimmer GmbH • Dover, OH, US
Quality Sr Engineer I

Quality Sr Engineer I

Zimmer GmbH • Dover, OH, US
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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. We focus on development opportunities, employee resource groups (ERGs), flexible work environments, competitive total rewards, wellness incentives, and a culture of recognition and performance awards. We are committed to creating an inclusive environment where every team member feels respected, empowered, and recognized.

What You Can Expect

Responsible for ensuring products conform to requirements and standards through audit, inspection, and testing activities. Interacts with various departments, suppliers, and external experts to meet Zimmer Biomet quality goals.

  • Supplier Qualification
  • Supplier Corrective Action
  • Supplier Change Notification
  • Supplier Production Part Approval
  • Supplier Performance Monitoring
  • Supplier Review Board
  • Supplier NCRs
  • Ensuring site KPIs are met

How You'll Create Impact

  • Develop and implement corrective / preventive action plans
  • Process supplier change notices
  • Create and execute supplier assessments and quality agreements
  • Ensure suppliers have necessary information and facilities to deliver quality products
  • This list is not exhaustive and may not include all duties for the Americans with Disabilities Act.

    What Makes You Stand Out

  • Ability to work collaboratively with teams and build relationships with suppliers and regulatory agencies
  • Results-oriented with ability to meet deadlines
  • Effective communication skills at multiple levels of the organization
  • High potential for future growth
  • Proficiency in Microsoft Office Suite
  • Basic knowledge of blueprint reading, geometric dimensioning and tolerancing, QSR / ISO regulations, design assurance, FMEA, and product testing methods; ability to use optical comparators and CMMs
  • Your Background

  • B.S. in engineering or related field; certification as a quality engineer (e.g., CQE) preferred
  • 3-5 years of relevant experience preferred
  • Certified Quality Engineer (CQE) and experience in the Medical Device or Orthopedic Industry preferred
  • Combination of education and experience may be considered
  • Travel Expectations

    Up to 20%

    EOE / M / F / Vet / Disability

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    Sr Quality Engineer • Dover, OH, US

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