Process Improvement Associate - Pharma Manufacturing

Novo Nordisk; Clayton (NC); On-site; USD 50,000 - 75,000; Full time

Benefits offered by this job

Leading pay and annual bonus

Paid time off with 14 holidays

Health, Dental, Vision insurance – day

8% 401K match

Family focused benefits: 14 weeks paid

Free access to Novo Nordisk products

Tuition assistance

Life & Disability Insurance

Employee referral awards

Job summary

Novo Nordisk, in Clayton, NC, is seeking a manufacturing support role to help supervise people, equipment, and processes across operations while meeting regulatory requirements. The position collaborates with production and QA on deviation investigations, containment, and root cause analysis.

Responsibilities include ensuring standards compliance, identifying improvement opportunities, performing process confirmations, reviewing BPRs, and adhering to safety and environmental guidelines in a

Qualifications

• Associate’s degree in technology or related field is required.
• High School Diploma or equivalent with a minimum of two years manufacturing experience is acceptable.
• Minimum of one year of manufacturing experience is preferred.
• Excellent written communication skills are required.
• GMP knowledge is preferred.
• System knowledge is preferred.
• Manufacturing experience is preferred, pharmaceutical manufacturing a plus.

Responsibilities

• Support people, equipment, and processes for operations areas to meet requirements.
• Work directly with production and QA to support deviation investigations, containment and root cause analysis.
• Ensure compliance with standards.
• Identify process improvements for routine to minimally complex matters.
• Perform process confirmations to ensure compliance and improvements.
• Review BPRs as necessary.
• Follow safety and environmental requirements.

Skills

Excellent written communication

GMP knowledge

System knowledge

Manufacturing experience

Pharmaceutical manufacturing

Education

Associate’s degree in technology

High School Diploma or equivalent with manufacturing experience

Job description

Novo Nordisk, in Clayton, NC, is seeking a manufacturing support role to help supervise people, equipment, and processes across operations while meeting regulatory requirements. The position collaborates with production and QA on deviation investigations, containment, and root cause analysis.

Responsibilities include ensuring standards compliance, identifying improvement opportunities, performing process confirmations, reviewing BPRs, and adhering to safety and environmental guidelines in a