Agilent seeks a Process Engineer to support GMP manufacturing operations at its Boulder, Colorado facility, focusing on oligonucleotide therapeutics. The role involves process engineering across upstream, midstream, and downstream operations, capital project management, regulatory compliance, and continuous improvement initiatives.
Responsibilities
- Provide process engineering support for GMP manufacturing including upstream, midstream, downstream, and utility systems
- Serve as engineering owner for designated process areas with technical support, monitoring, troubleshooting, and optimization
- Support capital projects through all phases including specification, procurement, installation, commissioning, and qualification
- Collaborate on technical transfer and process scale-up activities with development and manufacturing groups
- Drive continuous improvement initiatives through root cause analysis, data-driven decisions, and corrective actions
Requirements
- Bachelor's or Master's degree in Chemical, Mechanical, or Electrical Engineering or equivalent
- 4+ years pharma/biopharma and fine chemicals industry experience
- 3+ years with process/instrumentation diagrams, facility layouts, equipment sizing, URSs, SOPs, troubleshooting
- Multi-disciplinary team collaboration and hands-on problem-solving ability
- Familiarity with ASME BPE standards, NFPA/NEC electrical codes, and building codes
- Project management experience in biopharma preferred
- SCADA, PLC, and BAS design/programming experience preferred
Compensation: $103,200.00 - $161,250.00/yr plus benefits eligibility
Process Engineer in boulder at Unknown Company
This position is listed as full time and onsite.