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Sr Associate QA - AFP

Thousand Oaks, CA
Day to Day Responsibilities:
  • Drive and personally execute the implementation tasks of External Supplier Quality improvement projects
  • Basic understanding of the cGMPs
  • Working understanding of project management
  • Follow Current Good Manufacturing Practices (cGMP) regulations and Amgen policies and procedures
  • Work both independently and in a team environment
  • Able to follow step-by-step instructions, revise cGMP documentation and perform repetitive functions consistently and accurately
  • Work in a rapidly changing and demanding environment
  • Strong attention to detail, including the ability to proofread documents and accurately transcribe data
  • Additional projects, as assigned;
  • Administrative support experience;
  • Experience using MS Outlook, SAP/ERP Word, Excel, and PowerPoint in an office setting
  • A successful candidate will provide project management support and execution of tasks to drive the implementation of assigned projects and key deliverables in Amgen’s External Quality organization.
  • Working cross functionally with Contract Manufacturing and Raw Material organizations to execute projects related to External Supplier Quality and improvement of our cGMP Quality Systems.
"This posting is for Contingent Worker, not an FTE"
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