Location: REMOTE
Description:
Responsibilities:
• Develop and maintain applicable standard operating procedures, forms, and/or business documents: Acquire CDOCS editor access, revise controlled documents, manage document approval flows
• Develop and maintain key performance indicators (KPI's) and metrics for area management: Manage SKP reports, drive resolution to data errors, assist in developing metrics in Smartsheet
• Perform User Acceptance Testing: Acquire ALM tester access and support ALM testing requirements as required
• Contribute to cross functional projects
Basic Qualifications
• Master's Degree
• OR Bachelor's Degree and 2 years of Life Science or Business experience preferably in the biotechnology or pharmaceutical industry
• OR Associate's degree and 6 years of Life Science or Business experience preferably in the biotechnology or pharmaceutical industry
• OR High school diploma/GED and 8 years of Life Science or Business experience preferably in the biotechnology or pharmaceutical industry
• Excellence in working with MS Office
Preferred Qualifications
• Ability to learn new tasks, functions and responsibilities quickly
• Continuous improvement mindset
• Analytical reasoning and creative problem-solving ability to conceive the solutions of tomorrow
• Good negotiation and facilitation skills
• Demonstrated skill to handle multiple responsibilities and priorities simultaneously in a fluid environment with time pressures
• General understanding of regulatory guidelines impacting supply (i.e. GxP, SOX)
• High attention to detail
• Ability to operate in a team or matrixed environment
• Advanced skills using Amgen systems such as SAP, Microsoft Office Suite, CDOCS, Smartsheet, ALM and data visualization software
• CPIM certification
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