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Process Engineer – Biologics

Listing for: Intellectt Inc
Full Time position Listed on 2026-11-08
Job specializations:
  • Engineering
    Process Engineer, Validation Engineer, Quality Engineering, Pharma Engineer
  • Manufacturing / Production
    Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 120000 - 180000 USD Yearly USD 120000.00 180000.00 YEAR

Job Description & How to Apply Below

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.

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