Product Engineer 1

Duration: 12 months- potential to convert into full time

Description

Supports detailed manufacturing process objectives. Participates in the preparation and implementation of supply chain and manufacturing activities related to current and new products. 
Completes complex and detailed manufacturing process objectives. Completes the preparation of complex sketches, design layouts, and other specifications. Performs complex reviews of results to determine that the process follows proper procedure. Completes standardization of complex materials, components and assemblies. Completes and maintains detailed and comprehensive records of all inventive ideas, designs, and basic improvements. Completes product issues documentation for future reference and problem resolution. 

REQUIRED EDUCATION 
-BSME or BSEE or BioMedical Degree with 2 to 5 years experience in a FDA regulated medical devices environment OR manufacturing environment. 

MANDATORY SKILLS: 
This person involves heavy face-to-face and team interactions where good communication skills and interpersonal skills are needed. Creating meetings, presenting and obtaining consensus from a group is key.

REQUIRED SKILLS 
-Demonstrated knowledge of the limitations of all forms of current fabrication processes 
-Experience with design, manufacturing tools & principles involved in the production of precision devices, production processes, quality control, costs, and other techniques for maximizing the effective manufacture of high quality goods such as “Lean” and Design for Manufacturing and Assembly. 
-Experience developing, evaluating and improving manufacturing methods, utilizing knowledge of product design, materials and fabrication processes, tooling and production equipment capabilities, assembly methods, and quality control standards. 
-Interface experience with R&D, Supply Chain, Quality and Regulatory functions. 
-Experience with Excel Macros, Data Mining, PIVOT Tables and Charts. 
-Working knowledge of SAP is a Plus 

RESPONSIBILITIES 
-Work with R&D to develop quality designs that are manufacturable, testable, lowest cost and able to be global sourced over the life of the design. 
-Participate in R&D design reviews to ensure designs are quality, manufacturable, testable and lowest cost. 
-Coordinate supplier interface and participation during design & layout reviews for manufacturing. 
-Review design documents for compliance to design standards. 
-Work with R&D to minimize the use of special material, components, hardware and processes except where required by functionality and availability of alternative choices. 
-Complete all work required for design changes per the applicable design change process. 
-Review Component, Assembly drawings and Bills of Material, and other design documents looking for design completeness, design quality, component commonality with other designs, minimum or no high tolerance components and minimize the use of single source and high cost components. 
-Review design documents for compliance to design standards 
-Work with R&D to update and develop design standards based on manufacturing standards. 
-Work with R&D and the Tester Development Team to implement test equipment both internally and externally. 
-Work with Supplier Operations to establishing supply chain strategies and their implementation. 
-Work with Supplier Operations and Commodity managers to select supplier and place prototype orders 

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