• Sr. R&D Engineer

    Date:2022-04-06 00:00:00

    Job Responsibility:

    • Customer Requirement Collection and Analysis. 

    • Interface with clinicians to identify unmet clinical needs. 

    • Gather input from clinical, marketing, literature and other sources.

    • On market product’s benchmark. 

    • Hands-on work to build early concept prototypes.

    • Advanced material definition and Supplier selection, design phases component quality management. 

    • Product concept creation, selection and refine. 

    • Modeling and Drawing review and release, component specification creation and release.

    • Product specification definition and maintenance. 

    • Technical feasibility analysis and tests.

    • Design, develop, and refine new products and processes in R&D lab.

    • Develop and validate test methods.

    • Conduct design verification and validation, including animal study and physician validation.

    • Write and execute test protocols, analyze test data, write test reports.

    • Perform User and Design FMECA.

    • Create procedure, BOM, router, draft drawings compliant to standards with Cross functional support.

    • Identify process requirement, development and improve process parameters with Cross functional support. 

    • Identify problems and recommend solutions, continue design optimization.

    • New idea collection during projects execution. 

    • Patent draft and application.


    Qualification:

    • Minimum bachelor in engineering or similar,Master is a plus. 985,211 university is a plus.

    • 5 years of experience in medical device process and design.

    • Design thinking and design of experiments knowledge.

    • Experience with neurovascular implant processing and design is a plus.

    • Self-starter, driven to take initiatives to solve problems.

    • Ability to work independently and management time effectively.

    • Strong analytical, organizational skills and teamwork.

    • Proficient in Microsoft Office Suite, Adobe Reader, SolidWorks.

    • Understanding GMP and ISO 13485, FDA/CE regulatory requirements for product testing.

    • Presentation skill is a plus.

    • Proficient email communication with US/European suppliers in English.

    • Excellent verbal English, excellent vocabulary in technical neurovascular discussion is a plus.


    locations:

    Shanghai, China

    Email to:

    hr@taozhuang8.com

    ©2022 Wallaby Medical. All Rights Reserved     |   Privacy Statement     Official Wechat

    ©2022 Wallaby Medical. All Rights Reserved
    Privacy Statement
    Official Wechat