API Manufacturing Process Operator

Novo Nordisk A/S; Clayton (NC); On-site; USD 30,000 - 39,000; Full time

Benefits offered by this job

14 paid holidays

Health, dental, vision insurance on 1“

8% 401K company match

Parental & family leave: 14 weeks + 6

Free access to Novo Nordisk products

Tuition Assistance

Life & Disability Insurance

Employee Referral Awards

Job summary

Novo Nordisk in Clayton, NC seeks an Operations Technician to operate utility and RMS process equipment supporting API-US production. You will receive materials, complete training, and help meet environmental, health & safety and quality goals for the site.

Responsibilities include following SOPs for GMP and cGMP systems, recognizing and documenting anomalies, maintaining control systems, and performing site rounds with a focus on safe, compliant operations.

Qualifications

• High school diploma or GED required.
• Bachelor’s degree in a relevant field preferred.
• BioWork certification or equivalent a plus.
• Minimum of 6 months' experience in a regulated industry.
• Knowledge of utility and raw material systems in FDA/cGMP/OSHA environments is a plus.
• Experience with electronic batch records and DeltaV or Syncade preferred.
• Strong problem-solving using data-driven approaches.

Responsibilities

• Operate equipment and processes per SOPs for gMP and cGMP.
• Document anomalies for cause and clearance to minimize downtime.
• Maintain standards for automated and manual systems.
• Support site rounds and equipment inspections.
• Review electronic batch records in real time for compliance.

Skills

Problem solving

Electronic batch records

Communication

Teamwork

Education

Bachelor’s Degree in relevant field

BioWork certification

Tools

DeltaV

Syncade

Job description

Novo Nordisk in Clayton, NC seeks an Operations Technician to operate utility and RMS process equipment supporting API-US production. You will receive materials, complete training, and help meet environmental, health & safety and quality goals for the site.

Responsibilities include following SOPs for GMP and cGMP systems, recognizing and documenting anomalies, maintaining control systems, and performing site rounds with a focus on safe, compliant operations.