Biotech Downstream Manufacturing Associate (12h Shifts)

Scorpion Therapeutics

Holly Springs (NC)

On-site

USD 60,000 - 95,000

Full time

14 days+
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Job summary

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.

Qualifications

  • 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).

Responsibilities

  • 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.

Skills

NC BioWorks Certification
biotech/pharma industry experience
cGMP familiarity
EBR/MES experience
biologics process operations
manufacturing systems

Education

Bachelor's degree
Associate degree
High School diploma

Job description

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.

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