QA Specialist I

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.

San Diego, CA

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