Devon Bond Email & Phone Number

Atlanta, Ga, Us

Kennesaw, Ga, Us

Kennesaw, Ga, Us

Responsible for global technical product transfers to new or existing partners, manufacturing improvements, relationship management, supply chain continuity, and unit cost improvement

Kennesaw, Ga, Us

Managed process engineers in continuous improvement, cost savings, production development, and product line manufacturing support roles. I set departmental goals to achieve the company's strategic plan with a focus on project organization and prioritization across product lines and departments.

Kennesaw, Ga, Us

-Managed current and potential suppliers for cost savings and quality improvement opportunities-Engineering and Operations liaison for product manufacturing location transfer-Wrote and performed sustaining engineering feasibility, development, and verification protocols and reports-Initiated process improvement projects to improve efficiency of current manufacturing processes and reduce costs-Auditor for current and potential suppliers-Compiled and analyzed data to set action and control limits for new processes-Provided technical support for Tissue Processing Laboratory and medical device product lines-Assisted with implementation of new processes and equipment related to new product launches -Managed engineering change order and presented to Engineering Change Committee

Ann Arbor, Michigan, Us

-Led supplier change, new product development, and yield improvement projects to increase company profit-Project manager and lead engineer for creation of new product Design History Files (DHFs) with 510(k) submissions-Lead profitability projects with projected global annual savings of over $800,000-Complete all design control documentation such as new risk management file creation and design inputs/outputs-Audit new and current domestic and international suppliers and manage additions to approved supplier list-Evaluate potential projects using ROI, IRR, NPV, and payback period calculations-Lead design reviews and communicate team objectives, milestones, and progress of current projects-Identify and quantify cost savings opportunities and propose feasible projects to management-Manage current and potential suppliers for cost savings and quality improvement opportunities-Create CAD models, perform feasibility, design verification, validation, and design validation testing on new designs-Coordinate with mold suppliers and automation companies to create innovative in-mold assembly processes-Create and update project schedules based on changes in time, resources, and costs -Plan and perform usability studies with clinical staff including blood and animal testing-Track and report monthly savings of completed projects-Write and execute technical reports for acceptance criteria of supplier changes or new products-Monitor current inventory levels with implementation of new products to follow supply chain trends-Complete compliance related activities as requested

Ann Arbor, Michigan, Us

-Supervised second shift associates in blood monitoring product lines-Interviewed, trained, and approved associate competencies on various manufacturing processes-Updated and tracked waste in various steps of the manufacturing process to evaluate high fallouts and bottlenecks-Planned associates’ training schedules and rotations by organizing cross training to increase skill sets-Arranged associates based on efficiency rates and subassembly inventory levels to maximize product output-Wrote Nonconformance Reports, enforced quality bulletins, and updated deviations in production area-Identified root cause and implemented corrections for Nonconformance Reports-Managed associate timecards, wrote corrective action reports and discussed disciplinary actions with associates-Completed, investigated, and executed associate incident reports for associate’s safety-Isolated, segregated, and quarantined affected product during machine malfunctions-Updated production procedures to clarify process instructions and checksheets to document inspection criteria-Reviewed Device History Reports and yield reports for each lot of product

Ann Arbor, Michigan, Us

-Project lead of transferring products to in-house manufacturing production from third party supplier-Engineering representative in Off Pump Coronary Artery Bypass technology acquisition and product design transfer-Created multiple DHFs, Risk Analyses, Design Validations, Test Method Validations, and Operational Qualifications-Created and evaluated surveys sent to surgeons on usability of product line-Coordinated with third party suppliers on translations, IFUs, raw material specifications, and quality issues-Created new production and quality procedures and checksheets for new manufacturing processes-Trained quality, engineering, and incoming associates on new inspection methods-Completed ISO 11607 packaging validation testing for new packaging configurations-Aided in creation of new part numbers with new and modified BOMs, item maintenance, and routing documents-Completed investigation of Supplier NCR-Supported management in FDA and BSI audits-Completed and tracked projects with total annual savings of $660,000

Somerset, New Jersey, Us

-Assisted completing DOE and Gauge R&R studies for dilator tip forming machine replacement project-Performed testing and measuring products using Instron and Vision Measuring System-Drafted layout of New Engineering Laboratory

Internship on patient intake, device fabrication and modification, patient care observation and documentation.

Master Of Business Administration - Mba

Bachelor’S Degree, Biomedical Engineering

Globex Exchange Program