Process Improvement Associate I | Lean & QA

Biopharma Careers; North Carolina; On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Leading pay

Annual bonus

Paid time off

Health insurance from day one

Dental insurance

Vision insurance

401K with company match

Parental leave

Life & Disability Insurance

Tuition Assistance

Employee referral rewards

Job summary

Novo Nordisk in North Carolina seeks a manufacturing professional to support people, equipment and processes in our operations areas to meet business and regulatory requirements. You will provide process solutions for routine to moderate complexity issues and support training for junior team members.

Based in Durham at our Emerging Technologies - SDF US facility, the role emphasizes continuous improvement, data collection for reviews, and adherence to GMP.

Qualifications

• Bachelor’s degree in engineering, technology or related field.
• Manufacturing experience preferred, pharmaceutical environment ideal.
• Excellent written communication skills required.
• GMP knowledge required.

Responsibilities

• Work with production and QA to provide in depth deviation investigations and root cause analysis
• Drive continuous improvements via Lean tools
• Provide training on process and procedure changes
• Identify and implement process needs and improvement opportunities for routine to moderate complexity issues

Skills

GMP knowledge

Problem solving

Written communication

Education

Bachelor’s degree in engineering/technology

Associate’s degree with manufacturing experience

High School Diploma with manufacturing experience

Tools

SAP

PAS-X

Job description

Novo Nordisk in North Carolina seeks a manufacturing professional to support people, equipment and processes in our operations areas to meet business and regulatory requirements. You will provide process solutions for routine to moderate complexity issues and support training for junior team members.

Based in Durham at our Emerging Technologies - SDF US facility, the role emphasizes continuous improvement, data collection for reviews, and adherence to GMP.