Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Find Jobs
Find Jobs Near You – Available Work in Your Location
Skip to job details
CP
Commissioning Partners
Process Engineer
Review key factors to help you decide if the role fits your goals.
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
80
out of 100
Average of individual scores
Job Description
Process Engineer at Commissioning Partners Process Engineer at Commissioning Partners in Wilson, North Carolina Posted in 5 days ago.
Type:
full-time 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 c
GMP, 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.