Day-Shift Manufacturing Associate: Impact Patients

Amgen; West Greenwich (RI); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive benefits package

Discretionary annual bonus

Stock-based incentives

Generous time-off plans

Flexible work models (remote/hybrid)

Job summary

Amgen is seeking an Associate Manufacturing for day shifts in the U.S. You will operate in the Services Manufacturing area under supervision, following SOPs and contributing to critical processes such as weigh/dispense and cell bank work.

You’ll draft and revise procedures and reports, troubleshoot basics, and look for process improvements with Quality and Supply Chain support. The role requires foundational manufacturing experience (high school or higher) with GMP understanding, plus strong

Qualifications

• High school/GED with 2 years manufacturing or operations experience or Associate’s with 6 months experience or Bachelor’s.
• Ability to interpret and apply GMP knowledge.
• Understanding of analytical methods for manufacturing.
• Ability to demonstrate technical writing capability.
• Project management and presentation skills.
• Basic troubleshooting skills; experience with DeltaV.

Responsibilities

• Perform operations in the Services Manufacturing area under supervision.
• Work with SOPs; weigh/dispense, cell bank operations, equipment prep.
• Draft/revise Manufacturing Procedures, SOPs, and technical reports.
• Troubleshoot basics; review documentation for assigned functions.
• Identify improvements; collaborate with Quality, F&E, and Supply Chain.
• Represent manufacturing in cross-functional interactions.

Skills

GMP knowledge

Analytical methods

Technical writing

Project management

Presentation skills

Troubleshooting

Education

High school/GED + 2 years manufacturing or operations

Associate’s + 6 months manufacturing or operations

Bachelor’s

Tools

DeltaV

Job description

Amgen is seeking an Associate Manufacturing for day shifts in the U.S. You will operate in the Services Manufacturing area under supervision, following SOPs and contributing to critical processes such as weigh/dispense and cell bank work.

You’ll draft and revise procedures and reports, troubleshoot basics, and look for process improvements with Quality and Supply Chain support. The role requires foundational manufacturing experience (high school or higher) with GMP understanding, plus strong