Process Engineer I: Manufacturing & Process Improvement

Biopharma Careers; Iowa (LA); On-site; USD 85,000 - 115,000; Full time

Benefits offered by this job

Leading pay and annual bonus

14 paid holidays

Health, Dental, Vision from day one

8% 401K contribution

Parental & family medical leave

Tuition assistance

Life & Disability Insurance

Employee referral rewards

Job summary

Novo Nordisk, located in North Carolina, seeks a manufacturing support engineer to help ensure reliability of core processes and equipment. You will work to meet customer, business, and regulatory requirements while supporting validation activities and process improvements.

The role emphasizes cross-functional collaboration, quality focus, and the ability to operate in a 24/7 environment with safety and regulatory compliance at the forefront.

Qualifications

• Bachelor’s degree in Engineering/Science or related field required with 1+ year engineering/technical experience (GMP preferred).
• Associate’s degree with 3+ years of engineering/technical experience (GMP preferred).
• High school diploma with 5+ years of engineering/technical experience (GMP preferred).

Responsibilities

• Support validation & verification within area.
• Ensure quality of equipment and processes.
• Support process improvement projects for assigned area.
• Provide technical support to operating facilities to meet business goals.
• Generate ideas and support implementation for area improvements.
• Plan self-development with manager for career path.

Skills

Team collaboration

Regulatory knowledge (FDA)

Quality systems

Process improvement

Troubleshooting

Education

Bachelor’s Degree in Engineering, Science, or relevant technical field

Associate’s Degree in Engineering, Science, or relevant field

High School Diploma or equivalent

Tools

Process Control Systems

Job description

Novo Nordisk, located in North Carolina, seeks a manufacturing support engineer to help ensure reliability of core processes and equipment. You will work to meet customer, business, and regulatory requirements while supporting validation activities and process improvements.

The role emphasizes cross-functional collaboration, quality focus, and the ability to operate in a 24/7 environment with safety and regulatory compliance at the forefront.