Kelly Science, Engineering, Technology and Telecom, a managed solution provider and business unit of Kelly Services, is currently seeking a Staff Engineer for a long-term engagement at one of our Global Medical Device Manufacturing clients located in Irvine, CA .
Our Client is a global leader in the science of diagnosing and treating heart rhythm disorders. The company partners with clinicians to develop innovative technologies that improve the quality of care for arrhythmia patients worldwide
This role is a full-time, fully benefited position. As a Kelly employee, you will be eligible for Medical & Dental 50% paid, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation and sick/personal time. All KellyOCG employees receive annual performance reviews.
Staff Engineer-Project Manager
The Staff Engineer will be dedicated to new products, NPD , and existing product portfolio engineering cost improvement activities, including but not limited to the t esting and design change and validation . The Staff Engineer will lead the project from feasibility to commercialization. The Staff Engineer will collaborate with cross-functional departments and project manage overall project including feasibility, components qualification, supplier qualification, and implementation.
Responsibilities:
• Responsible for the cost reduction efforts of all products, materials, and techniques using engineering principles and financial impacts.
• Lead multiple projects that may deal with design/process change of medical device components.
• Work with cross-functional teams and coordinate design, development, and supplier quality activities as part of the project.
• Responsible for planning, developing, coordinating, and directing a large important engineering project or a number of small projects with many complex features.
• To manage the customer-specific requirements and offer technical support. Work on multiple phases or sub-tasks of projects or entire projects of moderate complexity, with results impacting project completion.
• Develop, design and propose concepts leveraging alternate manufacturing methods and/or material for high-cost components/assemblies.
• Perform engineering feasibility study for concepts proposed and demonstrate feasibility with data, samples, simulations or prototypes.
• Communicate with external suppliers to identify vendor sources for proposed design fabrication.
• Collaborate with various cross-functional teams to get design changes approved .
• Perform product cost improvement evaluation activities on mechanical designs.
• Support design change-related activities and documentation for the medical industry .
• Create and maintain Project Management files and communicate progress.
• Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work.
• Requires the use of advanced techniques and the modification and extension of theories, precepts, and practices of his/her field and related sciences and disciplines.
• Responsible for communicating business-related issues or opportunities to the next management level.
Requirements:
• A Bachelor’s Degree in Engineering (mechanical, electrical) is required.
• A minimum of 6-8 years of medical device work experience is required.
• Must possess a clear mastery of theoretical and practical fundamentals and experimental engineering techniques.
• Knowledge of drafting software systems such as AutoCAD and SolidWorks is preferred.
• Knowledge of statistical software packages such as Minitab is required.
• Project Management is required; FPX or PMP is preferred.
• Process Excellence such as Lean and Six Sigma certification preferred.
• Ability to travel up to 10% domestic
• Led a long-term project from feasibility to commercialization
Important information: Applicants must be legally permitted to work in the United States immediately and without employer sponsorship.
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