Senior QC Associate — Raw Material Testing Lead

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

Benefits offered by this job

Retirement plan

Health coverage (medical/dental/vision

Life and disability insurance

Flexible spending accounts

Annual bonus program

Stock incentives

Time-off plans

Flexible work model

Job summary

Amgen Rhode Island is seeking a Senior Associate Quality Control to support QC Centralized Raw Material Testing in the Wet Chemistry Laboratory. The role focuses on performing routine tests, maintaining schedules, and ensuring compliance with cGMP and quality standards.

The incumbent will generate accurate documentation, operate laboratory instruments, and collaborate with CTL and other teams to ensure timely results and continuous improvement in a highly regulated environment.

Qualifications

• Master’s or equivalent in a science field or related discipline.
• Experience in quality, manufacturing, or operations preferred.
• Strong documentation and regulatory awareness.
• Ability to work in a regulated lab environment.

Responsibilities

• Ensures facilities, equipment, materials, and processes comply with safety, cGMP and regulations.
• Generates accurate laboratory documentation using electronic systems and notebooks.
• Operates laboratory equipment and performs routine raw material testing.
• Manages the Raw Material Testing Master Schedule and approvals of assays.
• Reviews/approves results in LIMS and interfaces with CTL.

Education

Master’s degree in science

Bachelor’s degree + 6 months QA/Manufacturing/Operations experience

Associate’s degree + 2 years QA/Manufacturing/Operations experience

High school diploma / GED + 4 years QA/Manufacturing/Operations experience

Tools

LIMS

Electronic lab notebooks

Job description

Amgen Rhode Island is seeking a Senior Associate Quality Control to support QC Centralized Raw Material Testing in the Wet Chemistry Laboratory. The role focuses on performing routine tests, maintaining schedules, and ensuring compliance with cGMP and quality standards.

The incumbent will generate accurate documentation, operate laboratory instruments, and collaborate with CTL and other teams to ensure timely results and continuous improvement in a highly regulated environment.