Quality Engineer II.

Medtronic
Plainfield, Indiana, US
Full-time

Careers that Change Lives

In this exciting role as a Quality Engineer II, you will have responsibility for day-to-day manufacturing floor support in a medical device manufacturing area that supports products.

A Day in the Life

Responsibilities may include the following and other duties may be assigned.

  • Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product.
  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place.
  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Designs or specifies inspection and testing mechanisms and equipment; conducts quality assurance tests; and performs statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in the areas of design, incoming material, production control, product evaluation and reliability, inventory control and / or research and development as they apply to product or process quality.

Must Have : Minimum Requirements

Bachelor’s Degree in Engineering, Science or technical field with 2+ years of work experience in Engineering and / or Quality OR Advanced Degree in Engineering, Science or technical field with 0 years of work experience.

Nice to Have

  • Audit Readiness (external and internal audit experience).
  • CAPA experience (owner of CAPAs).
  • Process improvements (creation and implementation of improvements).
  • Experience in a manufacturing environment.
  • Experience with creation and completion of change controls.
  • Medical devices or Pharma experience.
  • 30+ days ago
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