Pharma Process Improvement Associate

Novo Nordisk; Clayton (NC); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

Job summary

Novo Nordisk's PS AM facility in Clayton, NC seeks a Manufacturing Support role to assist operations, QA, and compliance. The position focuses on deviation investigations, process confirmations, and continuous improvement in aseptic manufacturing for injectable diabetes and obesity therapies.

The role emphasizes collaboration with production and QA, adherence to GMP, and travel up to 10% as needed. Qualified candidates have relevant manufacturing experience and strong written communication.

Qualifications

• Associate’s degree in technology or equivalent is required.
• HS diploma with two years of manufacturing experience may be considered.
• Minimum one year of manufacturing experience in a pharmaceutical environment preferred.
• Excellent written communication skills required.
• GMP knowledge is preferred.
• System knowledge is preferred.
• General manufacturing experience is preferred.
• Pharmaceutical manufacturing experience is a plus.

Responsibilities

• Support deviation investigations, quick containments and root cause analysis with production and QA.
• Ensure compliance with standards across operations.
• Identify process needs and improvement opportunities for routine to minimally complex matters.
• Perform process confirmations to ensure compliance and improvements.
• Review BPRs as necessary.
• Follow all safety and environmental requirements in duties.
• Other duties as assigned.

Skills

Excellent written communication

GMP knowledge

System knowledge

Education

Associate’s degree in technology

High School Diploma + 2 yrs manufacturing experience

Job description

Novo Nordisk's PS AM facility in Clayton, NC seeks a Manufacturing Support role to assist operations, QA, and compliance. The position focuses on deviation investigations, process confirmations, and continuous improvement in aseptic manufacturing for injectable diabetes and obesity therapies.

The role emphasizes collaboration with production and QA, adherence to GMP, and travel up to 10% as needed. Qualified candidates have relevant manufacturing experience and strong written communication.