Liquidia Technologies is a privately-held clinical stage company focused on advancing vaccines and therapeutics that leverage the PRINTtechnology for design and manufacture of engineered particles. The PRINTtechnology offers unprecedented control of particle size, shape and chemistry in a highly consistent and scalable manufacturing process. In addition to its own products, Liquidia licenses its PRINTparticle technology and its GMP manufacturing capabilities to support proprietary programs advanced by collaborators.
We are committed to advancing precisely engineered products that profoundly impacts the lives of patients.
Liquidia is proud of its cultural values and strives for excellence and innovation in everything that we do.
Liquidia was founded in 2004 on the discoveries of Professor Joseph DeSimone at UNC, Chapel Hill
We are located in Research Triangle Park, North Carolina.
For additional information, please visit www.liquidia.com
The Process Engineer will assist the Liquidia manufacturing team with various tasks and projects. Primary responsibilities include:
Work within cross-functional teams to develop processes for production of novel nano-materials
Work with team of engineers and technicians to manufacture materials to support preclinical and clinical R&D projects
Serve as lead manufacturing representative for one or more R&D project teams to develop process capabilities to ensure adequate material supplies to meet project objectives
Support R&D project teams through the use of process engineering tools such as root cause analysis, risk assessment and Six Sigma tools
Lead efforts in the transition for lab scale to commercial scale manufacturing
Lead small to medium scope projects including the evaluation and implementation of process changes to improve product quality, decrease cost, and improve manufacturing efficiencies
Design and execute detailed experimental plans
Maintain accurate, detailed documentation throughout all phases of process development
Communicate and suggest direction to external and internal partners
BS/MS in a technical discipline required. Engineering preferred
5+ years of experience in process development or manufacturing operations required in Medical Device, Pharma or other FDA regulated industry
Demonstrated aptitude for ?hands-on? experimentation with an exemplary history as a ?self-starter?
Knowledge of Six Sigma/Process Excellence Tools including DoE, process capability analysis, C/E Matrix, pFMEA, fish bone diagrams, etc preferred.
Mechanical aptitude is a must, experience in the troubleshooting of production equipment preferred
Experience with the design of equipment/fixtures to support both prototype and production scale a plus
Demonstrated experience in DOE including experimental design, execution, data analysis and results summation
Ability to summarize data and results for business and technical audiences
P.O. Box 110085
Research Triangle Park, NC 27709