Quality Control Associate - Days

Quality Control Associate supporting analytical testing in a cGMP bioanalytics laboratory at Amgen's Rhode Island facility. The role involves operating sophisticated laboratory equipment, generating accurate documentation, and conducting in-process, release, and stability sample testing while maintaining regulatory compliance.

Responsibilities

• Conduct analytical testing including in-process, release, and stability sample analysis using HPLC/UPLC and capillary electrophoresis
• Generate complete and accurate laboratory documentation using electronic systems and notebooks following cGMP standards
• Operate sophisticated laboratory instrumentation and equipment
• Review and approve assays, documents, and records to ensure compliance with regulations
• Alert management to quality, compliance, supply, and safety risks; support continual improvement initiatives

Requirements

• High school diploma or GED with 2 years quality experience, or Associate's degree with 6 months quality experience, or Bachelor's degree minimum
• Detail-oriented with strong organizational skills and ability to manage multiple tasks
• Proficiency in laboratory equipment operation and scientific data interpretation
• Strong written and oral communication skills
• Experience with HPLC/UPLC, capillary electrophoresis, or general chemistry methodologies (preferred)
• Familiarity with GMP/GDP practices and laboratory investigations (preferred)