Process Engineer – Biologics

Intellectt Inc; Wilson (NC); On-site; USD 120,000 - 180,000; Full time

Job summary

Intellectt Inc is seeking an experienced Process Engineer to support the design, installation, commissioning, qualification, and startup of a large-scale biologics drug substance facility in Wilson, NC. The role focuses on GMP process systems, technology transfer, CAPEX projects, and operational readiness.

You will collaborate with Manufacturing, Quality, Automation, Validation, Engineering, construction teams, and vendors to ensure compliant, efficient startup and ongoing operations.

Qualifications

• Bachelor’s degree in Chemical, Mechanical, Biochemical Engineering, or related field.
• 8+ years of GMP large molecule biologics process/plant engineering experience.
• Experience with greenfield or brownfield startup, commissioning and qualification.
• Willing to work onsite in Wilson, NC; US work authorization.

Responsibilities

• Support process equipment and systems from design through startup and operational handover.
• Troubleshoot equipment and process issues and implement engineering improvements.
• Serve as a technical resource for GMP biologics manufacturing systems.
• Support technology transfer, process-fit-to-plant assessments, and CAPEX execution.
• Coordinate with Manufacturing, Quality, Automation, Validation, Engineering, construction teams, and vendors.
• Ensure compliance with GMP, safety, quality, and project requirements.

Skills

Troubleshooting

Project coordination

Leadership

Communication

GMP knowledge

On-site work

Biologics knowledge

Education

Bachelor’s degree in Chemical, Mechanical, Biochemical Engineering

Job description

Seeking an experienced Process Engineer to support the design, installation, commissioning, qualification, and startup of a large-scale biologics drug substance manufacturing facility. The role will support GMP process systems, technology transfer, CAPEX projects, and operational readiness.

Key Responsibilities

• Support process equipment and systems from design through startup and operational handover.
• Troubleshoot equipment and process issues and implement engineering improvements.
• Serve as a technical resource for GMP biologics manufacturing systems.
• Support technology transfer, process-fit-to-plant assessments, and CAPEX execution.
• Coordinate with Manufacturing, Quality, Automation, Validation, Engineering, construction teams, and vendors.
• Ensure compliance with GMP, safety, quality, and project requirements.

Required Qualifications

• Bachelor’s degree in Chemical, Mechanical, Biochemical Engineering, or a related discipline.
• 8+ years of process or plant engineering experience in GMP large molecule biologics manufacturing.
• Experience with greenfield or brownfield facility startup, commissioning, and qualification.
• Strong knowledge of biologics drug substance processes, equipment, utilities, and automation.
• Strong troubleshooting, project coordination, communication, and leadership skills.
• Legally authorized to work in the United States and available to work onsite in Wilson, NC.

Preferred: Technology transfer, CAPEX, Lean/Six Sigma, advanced degree, or PE certification.

US-based travelers and candidates willing to relocate will be considered.