Senior QC Specialist – HPLC/GC Expert

Amgen SA; West Greenwich (RI); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Competitive benefits

Total Rewards Plan

Professional development opportunities

Job summary

Amgen is seeking a Senior Associate Quality Control in Rhode Island to perform analytical testing and data review in a fast-paced environment. You will work with HPLC, GC, GC-MS and ICP-MS instruments, ensuring accurate documentation and regulatory compliance across all QC activities.

Ideal candidates have strong experience with validated methods, laboratory investigations, and process improvements in a GxP setting, contributing to product quality and patient safety.

Qualifications

• Demonstrated laboratory technique with pipetting small volumes accurately.
• Experience executing analytical testing per Methods and/or Compendia.
• Experience with QC analytical systems and/or Quality systems.

Responsibilities

• Perform testing methods including HPLC, GC and GC-MS.
• Perform testing and data analysis for compendia, non-compendia methods, and routine laboratory procedures.
• Generate accurate and concise laboratory documentation using electronic systems and notebooks.
• Operate and maintain specialized laboratory equipment and instrumentation.
• Participate in laboratory investigations, inspections and audits.
• Stay in sync with safety guidelines, cGMPs and other applicable regulatory requirements.

Skills

Attention to detail

Experience in validated QC

Team collaboration

Quality documentation

Analytical thinking

Strong communication

Education

High school diploma/GED + 4 years QC experience

Associate's degree + 2 years QC experience

Bachelor's degree + 6 months QC experience

Master's degree

Tools

LIMS

HPLC/GC/ICP-MS instrumentation

cGMP/compliant documentation

Job description

Amgen is seeking a Senior Associate Quality Control in Rhode Island to perform analytical testing and data review in a fast-paced environment. You will work with HPLC, GC, GC-MS and ICP-MS instruments, ensuring accurate documentation and regulatory compliance across all QC activities.

Ideal candidates have strong experience with validated methods, laboratory investigations, and process improvements in a GxP setting, contributing to product quality and patient safety.