Quality Control Supervisor

About AbbVie
AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

Quality Control Supervisor

Summary:

Supervises the Quality Control team in the inspection and release of all incoming materials and manufactured & serviced products in compliance with specifications and procedures.

Essential Duties and Responsibilities include the following (other duties may be assigned.):

• Supervise a team of quality control technicians for incoming, in-process and final QC functions
• Train and develop the quality control team
• Manage daily quality control reports and Tier level meetings
• Promote a culture of quality and oversee quality control processes
• Manages nonconformance reports as necessary and work with quality engineers on resolution
• May perform other duties as assigned.
• Assure compliance with QSRs and ISO regulations in the performance of department responsibilities.
• Actively manage the continual improvement of QC processes to ensure full compliance to applicable regulations and site initiatives
• Support the transfer of new products into Production
• May perform visual, functional and dimensional testing on incoming materials
• May perform in-process and final QC inspections
• Perform other responsibilities to support the needs of the department as assigned

Qualifications
Qualifications:

• 3-7 years plus experience in quality inspection/release. Must have experience in an FDA regulated industry
• 2-3 years supervisory experience preferred
• Experience with common measurement and testing tools and equipment included but not limited to: automated machines, calibers, QC testing tools
• Electromechanical device experience a plus
• High school diploma or equivalent is required

Additional Requirements:

• Able to read and understand Device History Records, specifications and reports
• Able to demonstrate leadership and assignment of duties
• 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

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, 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.