logo

View all jobs

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
Summary
  • 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"
More Openings
Associate
Associate Scientist
CDM Systems Manager
Material Coordinator
Share This Job
Powered by