QC Associate
Amgen · West Greenwich, RI
QualityFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Quality Control Associate role in manufacturing operations performing microbiology and analytical testing, sample management, and equipment maintenance in a GMP-regulated environment. Position works 10-hour shifts Saturday-Tuesday supporting Amgen's biopharmaceutical production and environmental monitoring.
What they're looking for
- High school diploma or GED plus 2 years quality experience
- Associate degree plus 6 months quality experience, or Bachelor's degree
- Experience in regulated biotechnology or pharmaceutical laboratory environments
- Proficiency with microbiology test methods including bioburden and endotoxin testing
- Familiarity with laboratory information systems such as LIMS or LMES
- Ability to work designated 10-hour Saturday-Tuesday schedule
What you'll be doing
- Perform sample collection and handling for GMP manufacturing and environmental monitoring operations
- Execute analytical testing including bioburden, endotoxin, TOC, conductivity, and microbiological assays
- Operate and maintain specialized laboratory instrumentation and automated sampling systems
- Generate accurate documentation using electronic systems and laboratory notebooks
- Participate in laboratory investigations, audits, and maintain regulatory compliance
Privacy & handoff
This role links to Amgen's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.