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Define, plan and lead activities, including test method & measurement system design/development and validation, fixture design and testing optimization in support of Design Verification
Write detailed test procedures that evaluate product sub-systems and systems against documented requirements
Execute critical product functional testing and conduct statistical analysis of test results
Author verification or validation reports upon execution of respective tests
Participate in the planning and execution of technical project work involving the application of engineering first principles and advanced engineering methods to gain deep understanding of the underlying technical issues, and to propose design or test method improvements
Create and document novel test methodologies and make recommendations for product/design changes
Ensure compliance with Client quality policies, procedures and practices as well as with all local, state, federal and Client safety regulations, policies and procedures.
Requirements:
Bachelor’s degree in Mechanical Engineering, Materials Engineering, Biomedical Engineering with mechanical emphasis, Electrical Engineering or related field
Proficiency in the use of SolidWorks CAD, and experience with designing complex mechanical and/or electromechanical components or assemblies using SolidWorks
Proficiency in basic statistical techniques for Engineering, including calculation of Means, Standard Deviations, use of Hypothesis Testing, etc.
Familiarity with using Minitab for statistical analysis of product test data
Ability to work independently and juggle multiple priorities
Strong project management experience working with multiple partners concurrently
2 or more years of post-baccalaureate professional experience leading or supporting product development projects
Experience with planning and executing appropriate Measurement System Analysis
including Gage R&R, to establish test method suitability
Experience with injection molded plastics and high-volume disposables
Proficiency in executing scripts and performing data analysis with MATLAB
Solid understanding of regulatory standards applicable to design of medical devices, including FDA QSR 21 CFR 820, ISO 13845
Nice to have:
Knowledge of intermediate or advanced statistical techniques
including familiarity with analysis of variance (ANOVA), Gage Repeatability and Reproducibility (Gage R&R) and design of experiment (DOE) methodologies