Manufacturing Process Engineer
RALEIGH, North Carolina
Job Id:
154792
Job Category:
Job Location:
RALEIGH, North Carolina
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Piper Enterprise Solutions
Position Owner:
Grace Patrick
Piper Companies is seeking a Process Engineer located in the RTP (NC). The ideal Process Engineer would be manufacturing focused and would primarily be responsible for leading the design, installation, and optimization of equipment used in cell culture and fermentation processes, ensuring systems operate reliably and meet GMP and process performance standards.
Responsibilities of the Process Engineer:
- Lead the design, installation, and qualification of upstream processing equipment (e.g., bioreactors, mixing systems).
- Support commissioning and troubleshooting of equipment used in cell culture and fermentation processes.
- Collaborate with cross-functional teams to ensure equipment meets process and regulatory requirements.
- Author and review technical documentation including equipment specifications, protocols, and reports.
- Drive continuous improvement initiatives related to equipment performance and reliability.
Qualifications for the Process Engineer:
- 5+ years of experience working on manufacturing equipment and processes.
- Strong understanding of bioreactor systems, mixing technologies, and single-use equipment.
- Experience in a startup facility and previously supported a start to finish manufacturing process.
- Ability to understand and communicate between groups such as quality, maintenance, validation, etc.
- Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, or related field.
Compensation for the Process Engineer:
- Salary Range: $110,000-135,000/year
- Comprehensive Benefits: Sick leave if required by law, medical, dental, vision, 401K
This job opens for applications on 10/13/2025. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: Process Engineer, bioreactors, cell culture, fermentation, equipment validation, commissioning, qualification, GMP, single-use systems, process development, tech transfer, scale-up, cleanroom, biotechnology, pharmaceutical, FDA compliance, 21 CFR Part 11, process optimization, troubleshooting, mechanical engineering, chemical engineering, bioprocessing, validation protocols, IQ OQ PQ.
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