GMP Documentation & Quality Specialist
amgenNew Albany (OH)
About the role
Amgen Inc. in Ohio is seeking an experienced documentation professional to support GMP manufacturing. You will develop, review, and update SOPs, WIs, and protocols, manage deviations, CAPA and change controls, and provide clerical support for document control.
You’ll liaise with cross-functional teams to implement changes and drive training documentation and continuous improvement. The role emphasizes accurate record keeping, timely processing, and maintaining current GMP standards in a
Before you apply
Applying takes about a minute. These four things decide how fast it moves after that.
Your profile is current
It's what we read first. Occupations, seniority and locations matter more than a long history.
Two examples you can talk through
Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.
A number in mind
What you're on now and what would make you move. We negotiate better when we know both.
Your notice period
Employers plan around it, and it's the question that stalls offers most often.
Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.
More like this