API Manufacturing Technician I

Novo Nordisk A/S; Clayton (NC); On-site; USD 40,000 - 55,000; Full time

Benefits offered by this job

Leading pay and annual bonus

14 paid holidays

Health/Dental/Vision insurance fromDay

8% 401K match

Parental & family leave

Job summary

Novo Nordisk in Clayton, NC is seeking an API manufacturing operator to run highly automated production equipment and help drive production goals. You will work in a GMP environment, follow SOPs, review batch records in real time, and support qualification and validation activities.

The role emphasizes safety, quality, and teamwork within a fast-paced pharmaceutical manufacturing site. The team values meticulous attention to detail, adherence to ISO and cGMP standards, and proactive problem

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
• Experience following SOPs and safety guidelines preferred
• Ability to read and understand product documentation and SOPs with attention to detail

Responsibilities

• Operate API manufacturing equipment to achieve production goals
• Follow GMP, SOPs, and cGMP standards
• Review electronic batch records in real time for compliance
• Participate in qualification and validation activities
• Load/unload materials and assist maintenance as needed
• Maintain clean room areas and environmental monitoring

Skills

Computer literacy

Attention to detail

Reading and understanding SOPs

Troubleshooting

Teamwork

Safety awareness

Education

High school diploma or equivalent

Associate's Degree or higher in Tech/Science/Engineering

Tools

MS Office

Industrial control equipment

Job description

Novo Nordisk in Clayton, NC is seeking an API manufacturing operator to run highly automated production equipment and help drive production goals. You will work in a GMP environment, follow SOPs, review batch records in real time, and support qualification and validation activities.

The role emphasizes safety, quality, and teamwork within a fast-paced pharmaceutical manufacturing site. The team values meticulous attention to detail, adherence to ISO and cGMP standards, and proactive problem