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Associate Quality Assurance

Thousand Oaks, CA
Day to Day Responsibilities:    
  • Sample and/or Inspect material as it come into the warehouse
  • Attend daily team meeting
  • Elevate issues to manager and help resolve
  • Communicate with material planners
  • Ideal candidate- 1-3 years experience with GMP environment. Material Sampling and/or Inspection experience, Prior GMP experience, ERP / Inventory System experience.
  • Primary responsibilities of this position include inspecting raw materials, components, and labels. Additional responsibilities include generating/compiling quality data and reports (e.g. lot track/trace, incidents), document review, initiate incidents, as well as coordinate and compile general documents.
  • The role will also require staff to work with Material Planners and Vendor Management staff for issue resolution. All work is performed following GMP.
  • Skills:  quality assurance or manufacturing experience in the pharmaceutical or medical device industry.
  • Attention to detail.
  • Experience working with Inventory System (ERP). Office programs such as Outlook, excel and word. Good Communication skills

"This posting is for Contingent Worker, not an FTE"
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