Biotech Downstream Manufacturing Associate (12h Shifts)

Amgen Inc.; Holly Springs (NC); Presencial; USD 60 000 - 95 000; Tempo integral

Resumo da oferta

Amgen in North Carolina is seeking an Associate in manufacturing to support downstream drug substance operations at a new flexible, tech-enabled facility. You will help startup, ensure operational readiness and run routine biologics production, with 12-hour shifts in a 24/7 manufacturing environment.

You will perform cGMP-compliant downstream steps, participate in commissioning and qualification activities, and contribute to safety, quality and compliance within a fast-paced biotech setting.

Qualificações

• High School diploma + 2 years regulated manufacturing experience, or Associate’s Degree + 6 months, or Bachelor's Degree.
• NC BioWorks Certification preferred.
• Biotech/pharma industry experience with familiarity of cGMP and electronic systems (EBR/MES).

Responsabilidades

• Execute cGMP-compliant downstream processes—column packing, chromatography, TFF, viral filtration, and final fill—plus equipment setup, operation, monitoring and cleaning.
• Support plant startup, operational readiness and routine production of biologics.
• Participate in commissioning, qualification, troubleshooting and continuous improvement with focus on safety, quality and compliance.

Conhecimentos

NC BioWorks Certification

biotech/pharma industry experience

cGMP familiarity

EBR/MES experience

biologics process operations

manufacturing systems

Formação académica

Bachelor's degree

Associate degree

High School diploma

Descrição da oferta de emprego

Amgen in North Carolina is seeking an Associate in manufacturing to support downstream drug substance operations at a new flexible, tech-enabled facility. You will help startup, ensure operational readiness and run routine biologics production, with 12-hour shifts in a 24/7 manufacturing environment.

You will perform cGMP-compliant downstream steps, participate in commissioning and qualification activities, and contribute to safety, quality and compliance within a fast-paced biotech setting.