Qc Inspector Manufacturing

JOB DESCRIPTION

Overview  
 
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. This Client is a global animal health company dedicated to supporting customers and their businesses in ever better ways. Building on more than 65 years of experience, it deliver quality medicines, vaccines and diagnostic products, complemented by biodevices, genetic tests and precision livestock farming. 
 
 
Job Title: QC Inspector (Manufacturing)  
 
Location: Union City, CA 94587  
 
Duration: 6  Months   
 
Job Type: Contract   
 
Work Type: Onsite    
 
Shift: 7:00 am - 3:30 pm (Monday-Friday)  
 
 
 
Duties and Responsibilities:  
 
 
 
Perform inspections of purchased parts according to acceptance criteria using standard sampling plan  
 
 
 
Physical, mechanical and/or electrical measurements in compliance with the company Quality System  
 
 
 
Accurately document results of inspection / testing and maintain controlled document files, logs and test records  
 
 
 
Inspect cables per wiring configuration  
 
 
 
Initiate non-conformance process and assist in resolving non-conformances  
 
 
 
Monitor receiving inspection backlog  
 
 
 
Able to be flexible with the work schedule  
 
 
 
Process ERP transactions to segregate and disposition non-conforming product  
 
 
 
Other duties and responsibilities in the Quality Department as assigned  
 
 
 
  
 
Qualifications:  
 
 
 
Familiar with measuring equipment such as micrometer, caliper height gauges, plug gauges  
 
 
 
Able to lift at least 35 lbs.  
 
 
 
Strong attention to details and ability to understand and follow complex procedures.  
 
 
 
Working knowledge and experience in basic computer applications such as Microsoft Word, Excel and Outlook.  
 
 
 
Effective and clear written and verbal communication skills in English language.  
 
 
 
  
 
Education and Experience:  
 
 
 
High School Diploma or Equivalent. 
 
 
 
Preferred one year of experience in an FDA regulated environment and/or ISO 13485 standards in the medical device industry and/or in-vitro diagnostics preferred  
 
 
 
  
 
TekWissen   Group is an equal opportunity employer supporting workforce diversity