EBR & MES Manufacturing Associate — Flexible/Remote

Amgen; Holly Springs (NC); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Retirement & Savings

Medical, Dental & Vision

Life & Disability Insurance

Flexible Spending Accounts

Annual Bonus

Stock-based Incentives

Time-off & Shutdowns

Flexible Work Options

Job summary

Amgen North Carolina (ANC) is hiring for a Senior Associate Manufacturing to support Electronic Batch Records (EBR) during start-up. You will generate and validate EBRs, assist with PAS-X implementations, and help integrate MES functionalities across manufacturing areas, ensuring regulatory readiness.

The role emphasizes collaboration with operations and quality groups, with exposure to Lean tools, SOP creation, and training activities in a fast-paced biopharmaceutical start-up environment.

Qualifications

• High School/GED with 4+ years in manufacturing/ops or equivalent.
• Bachelor’s or Master’s degree with related experience considered

Responsibilities

• Generate Electronic Batch Records (EBR) using PAS-X; edit, troubleshoot, validate.
• Support implementation of MES integrations and functionalities.
• Troubleshoot and execute EBRs; maintain electronic batch records.
• Create and maintain EBRs; optimize for process requirements.
• Support Lean Transformation through EBR metrics and CI tools.

Skills

PAS-X

EBR generation

MES integrations

SOP creation

Cross-functional collaboration

Education

High School/GED + 4 years manufacturing/ops experience

Associate’s Degree + 2 years experience

Bachelor’s Degree + 6 months experience

Master’s Degree

Tools

SAP

EBR/MES

DeltaV

Electronic Quality Systems

Job description

Amgen North Carolina (ANC) is hiring for a Senior Associate Manufacturing to support Electronic Batch Records (EBR) during start-up. You will generate and validate EBRs, assist with PAS-X implementations, and help integrate MES functionalities across manufacturing areas, ensuring regulatory readiness.

The role emphasizes collaboration with operations and quality groups, with exposure to Lean tools, SOP creation, and training activities in a fast-paced biopharmaceutical start-up environment.