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Zimmer Biomet
Indiana, United States
3 days ago

Description

Job Summary

Formulates procedures, specifications, and standards for Zimmer products and processes; Provides leadership for quality engineering projects from concept through design, implementation, testing, documentation, support, and maintenance; 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; and Ensures that suppliers have necessary information and facilities to deliver quality products to Zimmer.
Education/Experience Requirements

Requires a Bachelor's degree or foreign equivalent in Engineering or related field and 3 years of experience in a Quality Engineering role or related field. Must have 3 years of experience in the following: applying corrective and preventative actions (CAPA/SCAR), product/process containment activities, root cause analysis, problem solving and risk management techniques to minimize quality risks; nonconformance evaluation and disposition nonconformance's per industry regulations and quality control procedures; using verification and validation concepts such as IQ/OQ/PQ in manufacturing and evaluating processes by conducting capability studies; 3 years formulating procedures, specifications, requirements and standards for acceptance of products and processes; delivering, meeting deadlines, and having results orientation, ability to work within a team environment and build relationships outside of the department as well as outside the company (supplies, regulatory, agencies, etc.); utilizing Microsoft office suite, expert knowledge of blueprint reading and geometric dimensioning and tolerancing, FMEA; using inspection methods for product verification, source inspection of product, and use of statistical sampling methods to confirm effectiveness; developing MDM solutions using technologies such as IBM infosphere, informatica MDM, SAP MDM or SAP MDG; and performing analysis, design, implementation and IT maintenance activities; Must have 2 years of experience in the following: utilizing knowledge of measurement system analysis (Gage R&R), statistical process control techniques to evaluate and control processes; reviewing disposition master validation plans, verification and validation protocols; leading projects impacting supplier processes by applying structured methodology to project management; conducting SPPA/PPAP, defining requirements for internal/external changes impacting supplier processes and establishing specifications for first article acceptance; and Must have 1 year of experience performing supplier and/or supporting internal audits.
Travel Requirements

Position requires up to 20% domestic/international travel.

Job Information

  • Job ID: 61037836
  • Location:
    Indiana, United States
  • Position Title: Quality Senior Engineer I (444301)
  • Company Name: Zimmer Biomet
  • Job Function: Other
  • Job Type: Full-Time

Please refer to the company's website or job descriptions to learn more about them.

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