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Quality Engineer

In Minnesota / United States

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Quality Engineer   

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JOB TITLE:
Quality Engineer
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
Plymouth Minnesota / United States

JOB DESCRIPTION :

Hello,

This is Venkat from Intellectt Inc. Please find the below position and let me know your response.

Role: Quality Engineer

Location: Plymouth, MN

Duration: 12+ Months

Description:

The purpose of this position is to initiate medical device quality assurance activities. These activities must be in accordance with FDA Quality System Regulation, ISO13485, and other international standards. This position will also support device complaint investigation and failure analysis as required.

Essential Duties and Responsibilities:

  • Develop incoming inspection processes and document incoming inspection activities. Provide in-process QA support to include inspection and document review. Complete final acceptance activities. Manage the sterilization process, including validations and product sterile loads.
  • Track nonconforming material and lead Material Review Board (MRB) efforts. Interface and take the lead QA role in interactions with suppliers, contractors, and consultants that supply components, subassemblies, and contract processing.
  • Lead complaint investigations on the returned products. Manage corrective action and quality improvement activities.
  • Manage aspects of internal quality system relating to receiving inspection, calibration, MRB, etc. Assist in the performance of quality system internal auditing. Support quarterly management review meetings. Establish, monitor, and evaluate quality system metrics.

Position Details

Apr 17, 2021
S16174660863033009
Minnesota / United States
Plymouth
A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Quality Engineer    Apply

Click on the below icons to share this job to Linkedin, Twitter!

Hello,

This is Venkat from Intellectt Inc. Please find the below position and let me know your response.

Role: Quality Engineer

Location: Plymouth, MN

Duration: 12+ Months

Description:

The purpose of this position is to initiate medical device quality assurance activities. These activities must be in accordance with FDA Quality System Regulation, ISO13485, and other international standards. This position will also support device complaint investigation and failure analysis as required.

Essential Duties and Responsibilities:

  • Develop incoming inspection processes and document incoming inspection activities. Provide in-process QA support to include inspection and document review. Complete final acceptance activities. Manage the sterilization process, including validations and product sterile loads.
  • Track nonconforming material and lead Material Review Board (MRB) efforts. Interface and take the lead QA role in interactions with suppliers, contractors, and consultants that supply components, subassemblies, and contract processing.
  • Lead complaint investigations on the returned products. Manage corrective action and quality improvement activities.
  • Manage aspects of internal quality system relating to receiving inspection, calibration, MRB, etc. Assist in the performance of quality system internal auditing. Support quarterly management review meetings. Establish, monitor, and evaluate quality system metrics.