Summary

What can I offer you?

Mechanical Engineer with 7 years total engineering experience; 4 recent years in the medical device industry.

What am I looking for?

Skills

Education

Cal Poly University

San Luis Obispo
Bachelor of Science in Mechanical Engineering
Concentration in Mechatronics
Minor in Mathematics

ASQ Silicon Valley Biomedical Division

UCSC - University of Santa Cruz

Medical Device Verification and Validation

Cadence Project Management Certificate

Minitab Training

DMAIC (internal training at MPC) and 20-hour online Minitab course which together included: DOE, Response Optimization, Gage R&R, t-test, f-test, Confidence Intervals, Process Capability (Cpk, Ppk), ANOVA, Correlation, poka yoke

Professional Experience

MedPlast – Medical Device Contract Manufacturing

Manufacturing Engineer (2/16 – current position)

Responsibilities

Develop processes and fixtures for medical device assembly and secondary processes from proof of concept through sustaining.

Accomplishments

Ramped up manufacturing of cord blood stem cell separation disposable. Up to 10 operators on the production line with a customer demand of up to 6,000 devices per month on the packaged device level. Defined visual standards. Internal auditor to assure ISO 13485 compliance.

Corpus Medical – Medical Device Contract Manufacturing

Manufacturing Engineer (5/15 – 12/15, 7 months)

Responsibilities

Develop manufacturing processes. Design and implement fixtures, tools, and semi-automated equipment. Set-up and maintain manufacturing lines. Manage resources and schedules.

Accomplishments

Successfully sustained an Electrophysiology 3D Rotor Mapping solution catheter for finding arrhythmia in the heart up to the packaged device level. The device was produced at a volume of 50 per week, with about 16 operators building the device (8 hours of labor per device). Improved overall company wide systems.

Modified Polymer Components – Medical Device Components Compression Molding

Development Engineer (4/12 – 2/15, 3 years)

Responsibilities

Owned several medical device projects at a time, for various medical device customers, with various end uses, from proof of concept to transfer. Responsible for entire project from: planning and designing, to making first 5 parts, developing and documenting process, troubleshooting, pFMEA’s, managing BOM’s, validation, and ultimately transferring.

Used Solid Works on a nearly daily bases to design dies, tooling, fixtures, ect. Beta tester for Solid Works EPDM implementation. Ensured tolerance stack up wasn't an issue between tooling and material. Frequently used PLC’s to control timing in the semi-automated manufacturing processes. Used machine shop to make fixtures and die’s. Suggested DFM changes to customers. Used Design Review process to implement feedback on making the process more manufacturable. Used customer requirements to implement inspection and testing procedures like pull/tensile test, bend test, and proof test. Used Minitab to show process capability (Cpk, Ppk), suggest tolerance intervals to customers, and analyze/run DOE results. Used many coatings and materials. Some exposure to geometric tolerancing. Internal auditor to assure ISO 13485 compliance.

Accomplishments

ConXtech - Construction

R & D Engineer, Detail Manager, IT (1/06 – 2/12, 6 years total, approx. 3 years engineering experience and 3 years IT)

Responsibilities

Lead Engineer for the electro-mechanical portion of projects. Managed and organized structural drawing standards. Maintained and improved ConXtech's IT infrastructure and desktop support.

Accomplishments


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