Manufacturing Associate - Bulk Drug Substance Manufacturing Services - Days

Scorpion Therapeutics; Holly Springs (NC); On-site; USD 42,000 - 64,000; Full time

Job summary

Amgen in North Carolina is expanding its facility and seeks a Manufacturing Associate to support bulk drug substance manufacturing. You will help prepare media and buffers, set up equipment, and perform routine GMP activities.

The role requires high school with experience or a degree, strong communication skills, and familiarity with batch records and manufacturing systems. On-site work with shift flexibility and overtime during startup.

Qualifications

• Requires High School/GED with 2 years in a regulated environment, or an associates/bachelor's degree with related experience.
• Proficiency in Microsoft Office and strong communication skills preferred.
• Knowledge of electronic batch records and manufacturing systems is preferred.

Responsibilities

• Perform weigh and dispense of raw materials.
• Support equipment sanitation and process operations.
• Ensure cGMP compliance and document activities.
• Collaborate with cross-functional teams during startup and steady-state production.

Skills

Strong communication skills

Microsoft Office

Electronic batch records

Manufacturing systems

Education

High School/GED

Associate's Degree

Bachelor's Degree

Job description

Role

Manufacturing Associate supporting bulk drug substance manufacturing at Amgen's North Carolina facility expansion, focusing on operational readiness, media/buffer preparation, equipment setup, and routine GMP manufacturing activities.

Responsibilities

perform weigh and dispense of raw materials, support equipment sanitation, execute process operations, ensure compliance with cGMP, document activities, and collaborate with cross-functional teams during startup and steady-state production.

Requirements

High School/GED + 2 years regulated environment experience, or Associate's Degree + 6 months, or Bachelor's Degree; strong communication skills; proficiency in Microsoft Office; knowledge of electronic batch records and manufacturing systems preferred.

High-value

biologics manufacturing, cGMP compliance, media/buffer prep, facility startup, 24/7 shift work, cross-functional collaboration during production ramp-up.

Work setup

on-site in North Carolina, with shift flexibility during startup and steady-state operations. Occasional non-standard hours and overtime required.