Night QC Analyst - GMP Analytical Testing

Amgen SA; West Greenwich, Northern (RI, KY); Hybrid; USD 70,000 - 90,000; Full time

Benefits offered by this job

Total Rewards Plan

Employee benefits package

Discretionary annual bonus

Stock-based incentives

Flexible work models

Job summary

Amgen Rhode Island is seeking an Associate Quality Control professional for the Nights shift to provide analytical testing support in a GMP environment. The role is part of QC Night Shift Team D (Tuesday–Friday, 10 PM–8 AM) and requires diligent time management and attention to detail to ensure compliant testing.

You will perform analytical testing, generate laboratory documentation, operate instruments, and participate in investigations and deviations as needed to support product quality and

Qualifications

• Bachelor’s degree or higher in a relevant field.
• Experience in GMP analytical laboratory environments preferred.
• Strong attention to detail and time management.

Responsibilities

• Perform analytical testing including time sensitive samples (Titer/ MMV/ Mycoplasma/ Endotoxin/ Bioburden/ TOC).
• Ensure facilities, equipment, materials, and processes comply with safety and cGMP requirements.
• Generate accurate laboratory documentation in electronic systems and notebooks.
• Operate laboratory equipment and instruments.
• Review and approve assays, documents, and records.
• Support troubleshooting and problem solving; alert management to risks.
• Assist in investigations and deviations as applicable.
• Complete required trainings and perform additional duties as assigned.

Skills

GMP Analytical Lab

Analytical Testing

QC Documentation

Time Management

Communication

Education

Bachelor’s degree

Job description

Amgen Rhode Island is seeking an Associate Quality Control professional for the Nights shift to provide analytical testing support in a GMP environment. The role is part of QC Night Shift Team D (Tuesday–Friday, 10 PM–8 AM) and requires diligent time management and attention to detail to ensure compliant testing.

You will perform analytical testing, generate laboratory documentation, operate instruments, and participate in investigations and deviations as needed to support product quality and