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QA Specialist I

$27 - $29 per hour
Temporary

Experis

Title: QA Specialist I
Location: San Diego, CA 92121
Duration: 6 Months
Work Arrangement: 100% Onsite
Pay Range: $27 - $29 per hour (W2)

We are seeking a “QA Specialist I” to join one of our leading healthcare clients.

Description
Responsibilities
  • Responsible for running in-process, stability/calibration, final release, and experimental devices.
  • Notifying appropriate personnel of results and completing all associated data and documentation.
  • Cross-trained on all processes including in-process, stability, calibration, and final release.
  • Able to solve process-related questions/problems and minor investigations.
  • Review device history records.
  • Train new employees/Quality Control Technician I.
  • Operate laboratory equipment safely, as trained and directed, in accordance with established practices.
  • Responsible for inventory of all testing related materials.
  • Demonstrates commitment to the development, implementation and effectiveness of Alere Quality Management System per ISO, FDA, and other regulatory agencies.
  • Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
  • Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company’s policies and practices; build productive internal/external working relationships.
  • Carries out duties in compliance with established business policies.
  • Other duties as assigned, according to the changing needs of the business.
Minimum Qualifications | Education/Experience
Minimum Education
  • High School/GED graduate or equivalent.
Minimum Experience
  • 2 - 5 years relative work experience.
Preferred Qualifications
  • BS in a science-related field.
  • 2 – 5 years of laboratory experience in quality control/assurance or a manufacturing environment, preferably invitro diagnostics.
  • Proficient with Microsoft Office Suite; strong knowledge of Excel.
  • Organized and detail oriented.
  • Ability to work in a team environment.
  • Able to multitask and adapt to changes in task priorities.


We are looking for the candidate who are eligible to work with any employers without sponsorship .

If you’re interested, please click “Apply” button.
Vacancy posted 1 day ago
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