API Manufacturing Technician I – Growth & Impact

Novo Nordisk A/S; Clayton, Northern (NC, KY); Hybrid; USD 42,000 - 64,000; Full time

Benefits offered by this job

Health Insurance

14 paid holidays

401K company match

Life & Disability Insurance

Tuition Assistance

Parental & family medical leave

Job summary

Novo Nordisk is seeking an API Manufacturing Operator for our Clayton, NC site to operate highly automated production equipment in a GMP-compliant environment. This role supports batch records, equipment setup, and production scheduling to meet goals.

The ideal candidate will have 2+ years in FDA-regulated manufacturing, strong problem solving, and proficiency with SOPs and safety guidelines. On-site work with comprehensive benefits and training opportunities.

Qualifications

• High school graduate or equivalent required.
• Associate's Degree or higher in Tech, Science, or Engineering preferred.
• BioWork or equivalent industrial, military or vocational training combined with experience preferred.
• Minimum two (2) years of manufacturing experience in FDA regulated environment preferred.
• Experience following SOPs and safety guidelines.

Responsibilities

• Operate API manufacturing equipment to achieve production goals.
• Real time review of electronic batch records for compliance with SOPs and cGMP.
• Setup, operate, monitor, and control highly automated processes and systems.
• Load and unload products from trucks and ISO containers as required.
• Execute production schedule and participate in qualification/validation activities.

Skills

Safety compliance

Problem solving

Attention to detail

Computer literacy

Reading SOPs

Education

High school diploma or equivalent

Associate's degree in tech/science/engineering (preferred)

BioWork or equivalent training (preferred)

FDA-regulated environment experience (preferred)

Tools

Microsoft Office

Lock Out Tag Out systems

Job description

Novo Nordisk is seeking an API Manufacturing Operator for our Clayton, NC site to operate highly automated production equipment in a GMP-compliant environment. This role supports batch records, equipment setup, and production scheduling to meet goals.

The ideal candidate will have 2+ years in FDA-regulated manufacturing, strong problem solving, and proficiency with SOPs and safety guidelines. On-site work with comprehensive benefits and training opportunities.