Manufacturing Engineer

The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.

The Manufacturing Engineer position performs a wide variety of technical duties to support manufacturing operations.

• Transfer and scale-up of new processes from Chemical Development into Manufacturing.

• Attend and participate in project team meetings to develop and execute project plans.

• Interface with Chemical Development and Manufacturing to ensure small-scale development activities will scale to manufacturing equipment and systems.
  Responsible for the review and approval of technology transfer documents from Chemical Development.

• Responsible for writing or reviewing new process documentation (master batch records or data capture forms) and automated equipment methods.

• Coordinate the revision of standard operating procedures (SOPs) as required to support the transfer.

• Scale-up existing processes in Manufacturing.

• Responsible for writing and/or reviewing; scale-up batch documentation, change controls and automated equipment methods.

• Coordinate the creation and/or revision of SOPs as required to support the scale-up.

• Responsible for the generation and/or review of batch summaries for all batches produced in the manufacturing facilities.

• Responsible for communicating future development requirements or opportunities to the project team.

• Assist manufacturing with problem-solving and trouble-shooting process or process equipment including interfacing directly with external vendors and customers to clearly and concisely discuss and resolve the issue to meet production timelines, quality policies, and customer expectations.

• Actively lead or participate in the investigation of major process deviations including providing technical assistance to Quality Assurance (QA) on the final product impact assessment and identification of root cause as necessary.

• Bachelor’s or Master’s Degree or equivalent

• 4+ years of relevant experience in technical operations or manufacturing

• Experience with technical transfer and supporting manufacturing troubleshooting

• Skilled in authoring batch records, change controls, deviations, SOPs, and CAPAs

• Prior experience in a GMP manufacturing facility preferred

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