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;
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"