AbbVie

*Quality Control Technician II

Employer
AbbVie
Location
Dublin, CA, United States
Posted
Nov 14, 2020
Ref
202076
Discipline
Quality, Quality Control
Required Education
Masters Degree/MBA
Position Type
Full time
Envision working with energetic colleagues and inspirational leaders. Now, place yourself in that mix; leading discussions, asking the right questions and driving results.

Quality Control Technician II

What Your New Manager Wants You To Know

I am looking for an experienced Quality Control Technician II who will be responsible for, but not limited to, performing inspections following procedures, specifications and applicable standards and regulations. Provide technical support to cross-functional teams as needed, identifies potential discrepancies and nonconformance and alert management.

YOU ARE more than just a title, YOU ARE...

A strategic thinker : Align and excite internal stakeholders to facilitate success through strong leadership, strategic thinking and personal drive.

First class team player : Collaborate across multiple disciplines to ensure compliance and ability to influence cross-functional teams and senior leadership.

You Will

  • Inspect items for dimensional accuracy, functional operation and cosmetic standards according to drawings, quality procedures, other standards and specifications, using measuring instruments and devices as required per established AQL levels
  • Perform transactions in the ERP system as required and route material for storage/distribution
  • Inspect and verify the product and documentation to release final product for shipment. Identify and record product or documentation quality issues.
  • Issue nonconformance reports as necessary and work with quality engineers on resolution
  • Audit manufacturing line, workstations and quarantine areas to ensure compliance to requirements.
  • Assist in maintenance and coordination of calibration system
  • Scanning and filing records
  • Travel between ZELTIQ locations as needed
  • Must be available to work overtime as requested by the supervisor. This may include nights, weekends, and holidays during times critical to our business
  • Identify areas for Quality Control Improvements
  • Any other tasks assigned by the supervisor.


Qualifications

You Bring
  • 2 plus years' experience in quality inspection/release, preferably in an FDA regulated industry
  • Electromechanical component inspection experience required
  • Experience with common measurement and testing tools and equipment
  • Must have a solid understanding of MS Office applications such as Outlook, Word and Excel
  • Able to read and understand Device History Records, drawings, specifications and reports.
  • Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies.


Job Type
Standard

Schedule
Full-time

Equal Employment Opportunity
At Allergan, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.