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Quality Engineer I

Zimmer Biomet

Warsaw, INJob$64–80K/yrSeen 1w agoSeen in employer's feed 5 days ago

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At a glance

Compensation
$64–80K/yr
Location
Warsaw, IN
Work Authorization
Not specified

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Job overview

The Quality Engineer I is an entry-level position responsible for assuring products conform to established requirements and standards through audit, inspection, and testing. The role works with functional departments, suppliers, and external experts to support quality goals. It formulates procedures and standards, develops corrective and preventive action plans, analyzes gauge and product data, identifies resources for new products, and ensures suppliers have the information and facilities needed to deliver quality products.

Skills & qualifications

RequiredNice to have

Skills

TeamworkRelationship BuildingDeadline ManagementResults OrientationCommunicationMicrosoft Office SuiteBlueprint ReadingGeometric Dimensioning and TolerancingQSR/ISO RegulationsDesign AssuranceFMEAProduct TestingOptical ComparatorsCMMs

Qualifications

Bachelor's in Engineering or Alternative Bachelor's With CQE CertificationCertified Quality EngineerMedical Device ExperienceOrthopedic Industry Experience

Full job description

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 talent 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 included, respected, empowered and recognised.

What You Can Expect

The Quality Engineer I is an entry level position responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. You will interact with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals.

How You'll Create Impact

  • Formulates procedures, specifications, and standards for Zimmer products and processes.

  • Develops and implements corrective/preventative action plans.

  • Collects and analyzes data for gauge and product evaluation.

  • Identifies critical personnel, gauges, procedures, and materials needed for the completion of new products.

  • Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer Biomet.

Your Background

  • Ability to work within a team environment and build relationships outside of the department as well asoutside the company (suppliers, regulatory agencies, etc.).

  • Ability to deliver, meet deadlines and have results orientation.Good communication skills, both orally and in written form to multiple levels of the company.

  • Demonstrated characteristics of high potential for future development opportunities.Good command of Microsoft Office Suite

  • Basic knowledge of blueprint reading and geometric dimensioning and tolerancing, basic understanding ofQSR/ISO regulations, design assurance, FMEA, and product testing methods, and are able to use opticalcomparators and CMMs.

Your Background

You hold a B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality

engineer (e.g. CQE).

Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred

Physical Requirements

Travel Expectations

  • Compensation range: 64K- 80 K USD Annually.

EOE/M/F/Vet/Disability

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