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Quality Engineer - 1 year contract

Req ID: J2257352

  • 地点
    梅佐维科, 提契诺, Switzerland
  • 类别 质量
  • 发表 2021年1月18日
  • 类型 全职工作

职位描述

Advance your career and move global healthcare forward. Join the world's largest healthcare design and manufacturing services company where we create, design, and manufacture products and solutions that improve patient health for the leading healthcare brands of the world.

To enhance our Quality Team, we are looking for:

QUALITY ENGINEER

will represent the quality function of technical support, in conjunction with other internal support groups, regarding issues affecting manufacturing.

Your Reponsibilities include and are not limited to:

  • Develop and maintain QA plans and process routings, which reflect intended/actual activities.

  • Provide support for all quoting activities by participation in initial process design, development, and implementation phases.

  • Evaluate and support inspection processes via inspection aids and instruction guidelines.

  • Provide trend analysis of defects occurring at the customer, supplier and internally.

  • Interface with all departments as applied to the Policies and Procedures with special regard to ISO, EN4600 and GMP documentation.

  • Serve as liaison between Jabil Circuit and suppliers or customers on quality related issues.

  • Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor.

  • Accountability and ownership for material identification, material segregation, classification of defect types including the successful application of these techniques on a day-to-day basis in manufacturing.

What will you bring

  • A minimum of a Bachelor’s Degree (or Equivalent), preferably in Engineering or related technical field; or equivalent combination of education and experience

  • Relevant experience in manufacturing/operations is a plus.

  • Technical training and experience using Statistics, Lean and Six Sigma Methodologies is preferred including Measurement System Analysis, SPC, DOEs, Reliability, etc.

  • Knowledge of measurement techniques/-methodologies and GD+T is preferred

  • Experience working in both an FDA and European regulatory environment is preferred.

What is like working with us:

  • International environment and network

  • On-job, in-class and online trainings

  • Celebrating learning and success

Interested? Please apply by clicking the button below

**Please ensure to attach full reference work certificates and cover letter**

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