Yuan Ji
Principal Scientist (Tech Lead Sme), Abbott Vascular R & d @Abbott
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WORK HISTORY
Principal Scientist (Tech Lead Sme), Abbott Vascular R & d @Abbott
Santa Clara, CA, US
Technical Lead to oversee the global product development of cardiovascular devices including guide wires, balloon dilatation catheters (BDC), drug eluting stents (DES), drug eluting bioresorbable stents (DRS), Drug Coated Balloons (DCB), vessel closure devices, vascular plugs, Intravascular Lithotripsy (IVL), etc.•SME to support cross-functional team activities including materials failure analysis, quality control, preclinical study, FIH/IDE clinical trial, regulatory submission.•Responsible for the materials development of next generation cardiovascular devices to treat coronary and peripheral artery diseases (CAD and PAD).
EDUCATION
Stony Brook University
Ph.D., Materials Science and Engineering
Beihang University
M.S., Materials Science
Beihang University
B.E., Polymeric Materials Engineering
ABOUT YUAN JI
Established R&D leader in MedTech industry with more than 20 years of experience in the product development of class II/class medical devices and drug-device combinational devices.•Ph.D. in Materials Science with specialties in polymer chemistry/physics, formulation chemistry, materials processing, coating, surface/bulk material characterization, structure-property relationship, etc.•Areas of expertise: Ophthalmic product development: Intraocular Lens (IOL), Soft Contact Lens (SCL), optical materials and process, hybrid lens materials, reactive mixture formulation design, thermal/uv curing process development, ophthalmic solution with aqueous surfactants and water-soluble polymers.Coronary and endo vascular product development: drug eluting stent (DES), bioresorbable drug eluting stent (DRS), Drug Coated Balloon (DCB), hydrophilic/hydrophobic medical coatings, guide wires, balloon dilatation catheters (BDC), vessel closure devices/bioresorbable sutures, vascular plugs, Intravascular Lithotripsy (IVL), etc.•Outstanding technical leadership, team management and communication skills to drive cross functional team efforts from concept feasibility to design control and transfer to manufacturing.•Extensive research experience in a GLP/cGMP environment, familiar with design control procedures under the quality system regulation.
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