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Title

Quality Assurance Specialist 

EOE StatementWe are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.
 
Full-Time/Part-Time -unspecified-  
Description

The QA Specialist I works within the Quality Assurance and Regulatory Affairs Team under the direction of the Quality Assurance Manger to monitor, facilitate and assure company compliance with FDA, GMP, ISO, CE, IEC, Canadian and international registration and product regulations required for worldwide medical device distribution and sales.

QA Specialist I Roles and Responsibilities

  • Complaint Handling Program
  • Nonconforming Product Program
  • Corrective & Preventive Action Program
  • Deviation Administration
  • Change Control Program
  • Document Control Program
  • Primary QA File Administration
  • Internal Audit Program
  • Training Program
  • Calibration Program
  • Weekly “Walk Around” Inspections
  • Label Control Program
  • Label Control Room Administration
  • Primary Product Release Coordination

 

Education

College degree in Biology, Chemistry, Bio-Technology, Medical Technology or a related field.

 
Location Independence, MO  

This position is currently not accepting applications.

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