Manager, C&Q Document Preparation (Manufacturing Support)

About the role

In this role, you will support the preparation, coordination, and delivery of commissioning and qualification lifecycle documentation supporting engineering projects and GMP manufacturing systems across Amgen operations. This position may support one or more areas including Drug Substance, Drug Product, Finished Drug Product & Packaging, or Facilities & Utilities.

What you'll do

• Support document development activities using approved templates, standards, and CoE procedures

What you need

• GMP
• Any graduate