Position Summary
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.
Process Engineer – Biologics in Wilson at Intellectt Inc
This position is listed as full time and onsite. It was posted yesterday.