API Manufacturing Technician I – Grow in Pharma

Novo Nordisk; Clayton (NC); On-site; USD 48,000 - 64,000; Full time

Benefits offered by this job

Performance bonus

14 holidays per year

Health Insurance

401K with company match

Parental & family leave

Job summary

Novo Nordisk in Clayton, NC is seeking an API Manufacturing Operator to operate high-automation production lines and ensure GMP-compliant manufacturing. The role emphasizes strict adherence to SOPs, batch records, and quality controls within a fast-paced pharmaceutical environment.

The position requires a high school diploma or equivalent, with preferred further technical education and 2+ years of FDA-regulated manufacturing experience.

Qualifications

• High school diploma or equivalent required.
• Associate degree or higher in tech, science, or engineering preferred.
• 2+ years manufacturing experience in FDA-regulated environment preferred.
• Ability to read and follow SOPs and product documentation.
• Computer literacy and ability to operate controlled manufacturing equipment.

Responsibilities

• Operate API manufacturing equipment to meet production goals.
• Follow GMP documentation and ensure product quality.
• Review SOPs and related documents as required.
• Real-time review of electronic batch records for cGMP compliance.
• Manage training plan and assist in qualification/validation activities.
• Setup, operate, monitor, and control highly automated processes and systems.
• Load and unload product from trucks and ISO containers.
• Assist with maintenance and troubleshooting.
• Maintain clean room areas and environmental monitoring.

Skills

Computer literacy

Attention to detail

Problem solving

Reading SOPs

Education

High school diploma or equivalent

Associate degree or higher in tech/science/engineering

BioWork or equivalent training

Tools

Microsoft Office

Manufacturing control software

Job description

Novo Nordisk in Clayton, NC is seeking an API Manufacturing Operator to operate high-automation production lines and ensure GMP-compliant manufacturing. The role emphasizes strict adherence to SOPs, batch records, and quality controls within a fast-paced pharmaceutical environment.

The position requires a high school diploma or equivalent, with preferred further technical education and 2+ years of FDA-regulated manufacturing experience.