Process Engineer, API Recovery — GMP & Process Optimization

Novo Nordisk A/S; Powhatan (NC); On-site; USD 75,000 - 105,000; Full time

Benefits offered by this job

Annual bonus

Paid holidays

Health insurance

Dental insurance

Vision insurance

401K match

Parental leave

Family leave

Product access

Tuition assistance

Life insurance

Disability insurance

Referral bonuses

Job summary

Novo Nordisk A/S in Clayton, NC is seeking an Associate Process Engineer for API recovery to support manufacturing operations and document design inputs and specifications. The role emphasizes GMP compliance, risk assessments, and collaboration with engineering and project teams.

Responsibilities include process optimization, FMEA input, and coordinating with site stakeholders to maintain schedules and ensure safety and quality in a fast-paced production environment.

Qualifications

• Bachelor's degree in engineering or related field required.
• Associate's degree with 2+ years engineering experience in GMP preferred.
• High School Diploma with 4 years engineering experience in GMP environment preferred.

Responsibilities

• Provide routine support and troubleshooting for the manufacturing facility.
• Review and approve design and requirement documents; review and approve technical specs.
• Input and review Process FMEAs and design documents; participate in project workshops.
• Coordinate with site stakeholders and ensure schedule adherence.
• Support Quality Risk Management and process risk assessments.

Skills

GMP knowledge

Process optimization

Root cause analysis

Documentation

Cross-functional collaboration

Education

Bachelor's Degree in Engineering or related field

Associate's Degree in Engineering (2+ years experience)

High School Diploma with 4 years experience

Tools

Process Control Systems

Design of Experiments

Job description

Novo Nordisk A/S in Clayton, NC is seeking an Associate Process Engineer for API recovery to support manufacturing operations and document design inputs and specifications. The role emphasizes GMP compliance, risk assessments, and collaboration with engineering and project teams.

Responsibilities include process optimization, FMEA input, and coordinating with site stakeholders to maintain schedules and ensure safety and quality in a fast-paced production environment.