Night Shift: API Manufacturing Associate I

Novo Nordisk A/S; Powhatan (NC); On-site; USD 54,000 - 76,000; Full time

Benefits offered by this job

14 paid holidays

Health Insurance

Dental Insurance

Vision Insurance

401K with company match

Parental leave

Family medical leave

Job summary

Novo Nordisk in Clayton, NC seeks an API Manufacturing Associate I (Night Shift) to operate automated manufacturing equipment and support production goals in a GMP environment. The role involves following SOPs, reviewing batch records, and participating in training and maintenance activities.

The position requires a high school diploma, with a preferred Associate’s degree and at least two years of FDA-regulated manufacturing experience.

Qualifications

• High school graduate or equivalent required.
• Associate's Degree or higher in Tech, Science, or Engineering preferred.
• BioWork or equivalent training with experience preferred.
• Minimum two years of manufacturing experience in FDA regulated environment preferred.
• Experience following SOPs and safety guidelines.
• Computer literacy including Microsoft Office.

Responsibilities

• Operate API manufacturing equipment to achieve production goals.
• Follow GMP and cGMP documentation and SOPs.
• Review SOPs and documents as required.
• Real-time review of electronic batch records for compliance.
• Participate in training, qualification, and validation activities.
• Set up, operate, monitor, and control automated processes.
• Load/unload materials and execute production schedules.
• Assist during equipment maintenance and troubleshooting.
• Maintain clean room areas and environmental monitoring.

Skills

Manufacturing experience

SOP adherence

MS Office

Reading technical docs

Quality systems

Education

High school diploma or equivalent

Associate's degree (preferred)

Tools

MS Office

GMP systems

Job description

Novo Nordisk in Clayton, NC seeks an API Manufacturing Associate I (Night Shift) to operate automated manufacturing equipment and support production goals in a GMP environment. The role involves following SOPs, reviewing batch records, and participating in training and maintenance activities.

The position requires a high school diploma, with a preferred Associate’s degree and at least two years of FDA-regulated manufacturing experience.