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Specialist - Manufacturing - Engineering Support
AmgenNew Albany, OH
Posted Sep 28, 2026
What you’d do
Support a manufacturing team in a GMP environment by drafting and revising SOPs, work instructions, protocols, reports and training material, and by owning quality records such as deviations, CAPAs and change controls. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.
You’ll need
- Science and/or engineering educational background
- GMP pharma and/or biotech industry experience
- Technical writing experience
- Experience with device assembly and packaging
- Quality records: deviations, CAPA, change control
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