Allergan Quality Control Technician II in Dublin, California

Quality Control Technician II

Dublin, California, United States at

May 23, 2018Post Date

180087Requisition #

Allergan plc (NYSE: AGN) is a bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world.

Allergan markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology, women's health, urology and anti-infective therapeutic categories. With commercial operations in approximately 100 countries, Allergan is committed to working with physicians, healthcare providers and patients to deliver innovative and meaningful treatments that help people around the world live longer, healthier lives every day.

Allergan is a company that will inspire you to aim high with your ambition. Where you can build bridges all over the world. Where you can power ideas that drive change. And where you will act fast and drive results for customers and patients. Power your future & join our bold team.

Position Overview

Responsible for the inspection and release of all incoming materials and final product including review of records and inspection of materials and product in compliance with specifications and procedures.

Main Areas of Responsibilities

  • Perform visual, functional and dimensional testing on incoming materials

  • 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, work stations and quarantine areas to ensure compliance to requirements.

  • Inspect in-process subassemblies

  • Assist in maintenance and coordination of calibration system

  • Scanning DHR’s

  • Travel between Zeltiq locations

  • Must be available to work overtime as requested by the supervisor. This may include nights, weekends, and holidays during times critical to our business such as month-end, quarter-end, and year-end


  • At least 2 years of experience in quality inspection/release, preferably in an FDA regulated industry.

  • Experience with common measurement and testing tools and equipment.

  • Electromechanical device experience a plus.

Preferred Skills/Qualification

  • Able to read and understand Device History Records, 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.


  • High school diploma or equivalent.

Equal Employment Opportunity Employer

Allergan is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other protected status.