Support Amgen's global Quality Control network by providing centralized document management expertise
Job Summary
Support Amgen's global Quality Control network by providing centralized document management expertise.
Responsible for end-to-end document lifecycle management, including creation, authorship, review, and revision for QC processes.
This position offers a unique opportunity to collaborate with QC teams across Amgen sites worldwide, contributing to process harmonization and continuous improvement.
Matching Summary
Support Amgen's global Quality Control network by providing centralized document management expertise.
Skills & Requirements
Must-have
Technical writing in regulated environment
cGMP regulations for Quality Control
Laboratory computer systems experience
Document lifecycle management
Environmental monitoring/microbiology assessments
Nice-to-have
Innovative thinking and process transformation
Operational Excellence initiatives
Drug substance and drug product QC processes
Navigating ambiguity and structured problem solving
Key Requirements
Microbiology and Environmental Monitoring experience
Quality Control laboratory experience
Degree in Microbiology or other Life Science
Minimum 2 years of experience with Doctorate degree
Minimum 6 years of experience with Master's degree
Minimum 8 years of experience with Bachelor's degree
Minimum 10 years of experience with Associate's degree
Minimum 12 years of experience with High school diploma/GED