Biotech QC Associate: Microbiology & GMP Testing

BioSpace; West Greenwich (RI); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Retirement plan

Health, dental & vision

Stock-based incentives

Paid time off

Flexible work models

Job summary

Amgen is seeking an QC Associate for Manufacturing to support a fast-paced GMP environment. You will perform microbiology and analytical testing, manage samples, and operate laboratory instrumentation in a dynamic team setting.

The role emphasizes data integrity, accurate documentation, and training compliance, with responsibilities spanning sample handling, testing, and participation in investigations as needed. A strong emphasis on safety and regulatory adherence is required.

Qualifications

• Bachelor's degree required; alternative paths with relevant quality experience accepted.
• Experience in GMP/quality environments; knowledge of regulatory requirements.
• Comfort with documentation and data integrity in a fast-paced lab.

Responsibilities

• Perform sample collection and handling to support GMP operations and environmental/Water monitoring.
• Conduct testing for bioburden, endotoxin, TOC, conductivity and MMV.
• Operate and maintain lab equipment and instrumentation; ensure proper data review and documentation.
• Maintain training and compliance with safety, cGMP and regulatory requirements.

Skills

GxP laboratory experience

Quality testing

Electronic systems proficiency

Laboratory instrumentation

Project management

Education

Bachelor's degree

Associates + 6 months quality experience

High school/GED + 2 years quality experience

Tools

LIMS

LMES

TrackWise

Job description

Amgen is seeking an QC Associate for Manufacturing to support a fast-paced GMP environment. You will perform microbiology and analytical testing, manage samples, and operate laboratory instrumentation in a dynamic team setting.

The role emphasizes data integrity, accurate documentation, and training compliance, with responsibilities spanning sample handling, testing, and participation in investigations as needed. A strong emphasis on safety and regulatory adherence is required.