Manufacturing Operator I (C Shift)

Scorpion Therapeutics; Durham (NC); On-site; USD 36,000 - 48,000; Full time

Job summary

Novo Nordisk in Durham, NC is seeking a Manufacturing Operator to operate and monitor production equipment for oral solid dosage products in a regulated pharmaceutical environment.

Responsibilities include setup, sanitation, and maintenance of lines, executing production schedules, handling labeling, adhering to SOPs, and upholding GMP compliance and safety standards on-site.

Qualifications

• High School Diploma or equivalent required.
• Associate’s Degree or Bioworks Certification preferred.
• Minimum one year of experience in pharmaceutical solid dose manufacturing or FDA-regulated industry preferred.

Responsibilities

• Setup, operation, sanitation, and maintenance of manufacturing lines.
• Execute production schedules and handle labeling and components.
• Adhere to SOPs and ensure quality compliance.
• Support equipment maintenance and safety protocols.

Skills

Product docs reading

Computer skills

Mechanical aptitude

Education

High School Diploma or equivalent

Associate’s Degree

Bioworks Certification

Job description

Role: Manufacturing Operator at Novo Nordisk's Durham solid dosage facility, responsible for operating and monitoring production equipment for oral treatments in a regulated pharmaceutical environment.

Responsibilities

Setup, operation, sanitation, and maintenance of manufacturing lines, executing production schedules, handling labeling and components, adhering to SOPs, ensuring quality compliance, and supporting equipment maintenance and safety protocols.

Qualifications

• High School Diploma or equivalent required;
• Associate’s Degree or Bioworks Certification preferred.
• Minimum one year of experience in pharmaceutical solid dose manufacturing or FDA-regulated industry preferred.

Skills

• ability to interpret complex product documentation
• computer proficiency
• basic mechanical aptitude preferred.

High-Value

focus on oral solid dosage forms, regulated manufacturing, compliance with GMP standards, and safety in a cGMP environment.

Work setup

on-site manufacturing with physical demands including lifting, standing for extended shifts, and potential work in cold, loud, or hazardous environments.