Pharma Manufacturing Operator I - Solid Dose Production

Novo Nordisk A/S; Durham (NC); On-site; USD 25,000 - 34,000; Full time

Job summary

Novo Nordisk is seeking an Production Operator to operate manufacturing equipment, support packaging lines and follow strict SOPs in a Durham, NC facility. The role emphasizes safety, quality, and adherence to production schedules.

You will read and follow complex documentation, participate in maintenance activities, and ensure accurate data recording while upholding GMP standards. This position offers growth in a global healthcare company with strong benefits.

Qualifications

• Ability to read, write & understand complicated product documentation and SOPs with attention to detail.
• Computer literacy including Microsoft Office programs.
• Basic mechanical skills preferred.
• High school diploma or equivalent required; associate degree or Bioworks certification preferred.

Responsibilities

• Setup, operate, monitor & control equipment, systems & processes.
• Clean & sanitize manufacturing, filling & packaging rooms & equipment per SOPs.
• Execute production schedule to achieve production goals.
• Handle labeling & components correctly; transferring, counting, FIFO, returns, etc.
• Participate in event response and support.
• Read & follow SOPs, job instructions and other documents to ensure compliance.
• Identify, report & resolve quality issues.
• Assist during equipment maintenance, including restoration of function and preventative maintenance.
• Record/review production data in appropriate forms.

Skills

SOP literacy

MS Office

Basic mechanical skills

Attention to detail

Read/write in reading product docs

Education

High School Diploma or Equivalent

Associate’s Degree or Bioworks Certification preferred

Job description

Novo Nordisk is seeking an Production Operator to operate manufacturing equipment, support packaging lines and follow strict SOPs in a Durham, NC facility. The role emphasizes safety, quality, and adherence to production schedules.

You will read and follow complex documentation, participate in maintenance activities, and ensure accurate data recording while upholding GMP standards. This position offers growth in a global healthcare company with strong benefits.