Senior QC Associate — Day Shift, Innovative Lab Impact

Amgen Inc.; West Greenwich (RI); Presencial; USD 79.000 - 107.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Retirement and Savings Plan

Medical, dental and vision coverage

Life and disability insurance

Flexible spending accounts

Annual bonus program

Stock-based incentives

Generous time-off plans

Flexible work models

Descripción de la vacante

Amgen Inc. in the United States is seeking a Senior Associate Quality Control to support analytical testing and data review in a fast-paced, GxP environment.

In this role, you will perform HPLC, GC and GC-MS testing, manage data, operate laboratory instruments, and participate in investigations and audits while upholding cGMP standards. A relevant degree and QA experience are required, with opportunities for professional growth and a strong benefits package.

Formación

• High school diploma or GED with 4 years of QA experience or equivalent combination.
• Associate's degree with 2 years QA experience or higher.
• Bachelor's degree with 6 months QA experience or higher.
• Master's degree or higher preferred.

Responsabilidades

• 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.

Conocimientos

HPLC

GC

GC-MS

Data analysis

cGMP

Educación

High school/GED

Associate's degree

Bachelor's Degree

Master's Degree

Herramientas

QC analytical systems

Quality systems

Descripción del empleo

Amgen Inc. in the United States is seeking a Senior Associate Quality Control to support analytical testing and data review in a fast-paced, GxP environment.

In this role, you will perform HPLC, GC and GC-MS testing, manage data, operate laboratory instruments, and participate in investigations and audits while upholding cGMP standards. A relevant degree and QA experience are required, with opportunities for professional growth and a strong benefits package.