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Process Engineer

Job in Wilson, Wilson County, North Carolina, 27893, USA
Listing for: Commissioning Partners LLC.
Full Time position
Listed on 2026-10-05
Job specializations:
  • Engineering
    Process Engineer, Validation Engineer, Pharma Engineer, Quality Engineering
  • Pharmaceutical
    Validation Engineer, Pharma Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 85000 - 120000 USD Yearly USD 85000.00 120000.00 YEAR
Job Description & How to Apply Below

We are looking for an experienced Process Engineer to support pharmaceutical manufacturing processes, equipment, process optimization, technology transfer, and validation activities.

Responsibilities:
  • Provide engineering support for pharmaceutical manufacturing and process operations.
  • Support process development, optimization, scale-up, technology transfer, and process improvement activities.
  • Troubleshoot process and equipment issues affecting quality, yield, throughput, and production performance.
  • Develop and review process flow diagrams, P&IDs, process descriptions, equipment specifications, and technical documentation.
  • Support equipment selection, installation, commissioning, startup, and qualification.
  • Participate in process validation, PPQ, engineering runs, and manufacturing readiness activities.
  • Support deviations, investigations, CAPA, change controls, and root cause analysis.

    Evaluate process performance and identify opportunities for improved efficiency, reliability, capacity, and cycle time.
  • Collaborate with Manufacturing, Quality, Validation, Maintenance, Automation, Engineering, and external vendors.
  • Support technology transfer and implementation of new processes and equipment.
  • Develop technical reports, SOPs, process documentation, and engineering deliverables.
  • Ensure process engineering activities comply with cGMP, FDA requirements, and site procedures.
Qualifications:
  • Bachelor's degree in Chemical, Mechanical, Biochemical, Pharmaceutical, or related Engineering discipline.
  • 3+ years of pharmaceutical, biotechnology, or regulated manufacturing experience.
  • Experience with pharmaceutical manufacturing processes and process equipment.
  • Knowledge of process validation, PPQ, technology transfer, and GMP requirements.
  • Strong troubleshooting, analytical, and problem-solving skills.
  • Experience with PFDs, P&IDs, process equipment, and engineering documentation.
  • Experience with upstream, downstream, formulation, fill-finish, or other pharmaceutical manufacturing processes is a plus.
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