Associate Document Control Coordinator

Location: Thousand Oaks, CA
Date Posted: 11-08-2018
Day to Day Responsibilities:     
  • Enter GMP data into SAP following Standard Operating procedures
  • Scanning and loading of documents into the Electronic Document Management System
  • Basic understanding of the cGMPs and project management
  • Follow step-by-step instructions and perform repetitive functions consistently and accurately
  • Work both independently and in a team environment
  • Follow Current Good Manufacturing Practices (cGMP) regulations and Amgen policies and procedures
  •  Work in a rapidly changing and demanding environment
  • Strong attention to detail, including the ability to proofread documents and accurately transcribe data into SAP
  •  Additional projects, as assigned; Skills: administrative support experience; experience using MS Outlook, SAP/ERP Word, Excel, and PowerPoint in an office setting
Summary:
  • A successful candidate will provide data entry, document management and administrative support to maintain Good Manufacturing Practices (GMP) in Amgen’s External Quality organization.
  • Responsible for GMP data entry and leveraging basic project management to track deliverables. Responsible for SAP master data entry and processing of GMP documents through the approval process in a confidential and secure manner.
  • Working cross functionally with Contract Manufacturing and Raw Material organizations to execute to day-to-day responsibilities within QMS related systems. Support key deliverables and / or projects as part of External Quality.

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