Pharma Manufacturing Process Specialist

Novo Nordisk A/S; Clayton (NC); On-site; USD 52,000 - 72,000; Full time

Benefits offered by this job

Annual bonus

14 paid holidays

Health Insurance

Dental Insurance

Vision Insurance

401K with company match

Parental leave

Family medical leave

Product access

Tuition assistance

Life & Disability Insurance

Employee referral awards

Job summary

Novo Nordisk is seeking a QA/Manufacturing support role at our Clayton, NC PS AM facility to assist with deviation investigations and process confirmations, ensuring regulatory compliance and product quality. You will collaborate with production and QA teams to identify improvements and maintain safe operations.

Qualified candidates have an associate degree in technology or equivalent, with manufacturing or GMP exposure preferred, and a willingness to travel up to 10% as needed.

Qualifications

• Associate’s degree in technology from an accredited university is required.
• High School Diploma or equivalent with 2 years of manufacturing experience may be considered.
• Minimum 1 year of manufacturing experience in a pharmaceutical environment preferred.
• GMP knowledge preferred.
• System knowledge preferred.
• Pharmaceutical manufacturing experience is a plus.

Responsibilities

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

Education

Associate’s degree in technology

High School Diploma or equivalent with 2 years manufacturing experience

Minimum 1 year manufacturing experience in pharma

GMP knowledge (preferred)

System knowledge (preferred)

Pharmaceutical manufacturing experience a plus

Tools

System knowledge

Job description

Novo Nordisk is seeking a QA/Manufacturing support role at our Clayton, NC PS AM facility to assist with deviation investigations and process confirmations, ensuring regulatory compliance and product quality. You will collaborate with production and QA teams to identify improvements and maintain safe operations.

Qualified candidates have an associate degree in technology or equivalent, with manufacturing or GMP exposure preferred, and a willingness to travel up to 10% as needed.