Process Engineer – Biologics

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.