This job is closed

We regret to inform you that the job you were interested in has been closed. Although this specific position is no longer available, we encourage you to continue exploring other opportunities on our job board.

Quality Engineer II

$76,000 - $114,000/Yr

Medtronic - Mystic, CT

posted 2 months ago

Full-time - Entry Level
Mystic, CT
10,001+ employees
Miscellaneous Manufacturing

About the position

The Quality Engineer II at Medtronic is responsible for supporting the ENT manufacturing process to ensure the highest reliability and quality of products. This role involves investigating nonconforming devices, implementing corrective actions, and identifying improvements to enhance production efficiency. The engineer will also monitor complaints related to surgical devices and collaborate with engineering and manufacturing teams to uphold quality standards.

Responsibilities

  • On-site support of daily manufacturing operations including troubleshooting of equipment, investigation of defects, and validation of equipment/processes.
  • Develop, modify, apply and maintain quality standards and protocol for processing materials into partially finished or finished products.
  • Collaborate with engineering and manufacturing functions to ensure quality standards are in place.
  • Devise and implement methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.
  • Design or specify inspection and testing mechanisms and equipment; conduct quality assurance tests; and perform statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.
  • Ensure that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.
  • May specialize in areas such as design, incoming material, production control, product evaluation and reliability, inventory control, and/or research and development as they apply to product or process quality.

Requirements

  • Bachelor's degree required
  • Minimum of 2 years of relevant experience, or advanced degree with 0 years of experience

Nice-to-haves

  • Bachelor's degree in engineering
  • Process Validation experience (MVP, IQ, OQ, PQ)
  • Quality systems and compliance experience
  • Experience in a Medical device Industry
  • Experience with NCMRs and CAPAs

Benefits

  • Competitive Salary
  • Flexible Benefits Package
  • Short-term incentive called the Medtronic Incentive Plan (MIP)
Job Description Matching

Match and compare your resume to any job description

Start Matching
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service