Pharma Solid-Dose Manufacturing Operator I

Novo Nordisk; Durham (NC); On-site; USD 23,000 - 34,000; Full time

Benefits offered by this job

Annual performance bonus

Paid holidays

Health, dental, vision insurance from‑

401K with company match

Paid parental leave

Tuition assistance

Life & Disability Insurance

Job summary

Novo Nordisk in Durham, NC seeks a Production Operator to operate manufacturing equipment and contribute to meeting daily production goals within our solid dosage facilities. You’ll follow SOPs, maintain cleanliness, and monitor equipment while upholding safety standards.

The role requires a high school diploma or equivalent, basic computer literacy, and attention to detail; GMP or FDA experience is a plus. We offer on-site schedule, benefits from day one, and career growth opportunities.

Qualifications

• High School Diploma or equivalent required.
• Associate's degree or Bioworks Certification preferred.
• Minimum of one year of experience in pharmaceutical solid dose manufacturing or other FDA regulated industry preferred.
• Ability to read, write & understand complicated product documentation & SOPs with attention to detail.

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.

Skills

Attention to detail

Reading & writing

Basic math

Computer literacy

Education

High School Diploma or Equivalent

Associate's Degree or Bioworks Certification

Job description

Novo Nordisk in Durham, NC seeks a Production Operator to operate manufacturing equipment and contribute to meeting daily production goals within our solid dosage facilities. You’ll follow SOPs, maintain cleanliness, and monitor equipment while upholding safety standards.

The role requires a high school diploma or equivalent, basic computer literacy, and attention to detail; GMP or FDA experience is a plus. We offer on-site schedule, benefits from day one, and career growth opportunities.