Title : Mechanical Design Engineer
Location: Sunnyvale, CA 94043
Duration: 6 Months
Job Description:
Designs and analyzes mechanical systems, equipment and packaging.
Conducts feasibility studies and testing new and modified designs.
Directs support personnel in the preparation of detailed design, design testing and prototype fabrication.
Provides design information to drafting for packaging documentation.
Min 3 Years of experience is required.
Primary Function of Position
Design and construct manufacturing equipment used to produce minimally invasive medical devices.
This equipment will range in complexity from custom manual fixtures to semi-automated electro-mechanical systems, integrating work-holding, sensing, motion and vision control.
This position will play a critical role in developing cutting edge manufacturing capabilities to enable the future of minimally invasive surgery.
The ideal candidate should have a solid understanding of the technical aspects of mechanical engineering and design. He/she will work closely with senior level equipment staff and other departments to develop and sustain custom equipment for production use.
This person will thrive working autonomously on projects with medium to high complexity.
Essential Job Duties
Design and build in-house manufacturing equipment from concept to implementation
Create effective design solutions of mechanical assemblies from simple fixtures to more complex assembly for automation equipment.
Iterate rapidly by prototyping, testing, and examining product designs using engineering methods and techniques, including computer simulation and physical models
Ensure manufacturing equipment designs meet functional, safety, ergonomic, documentation, and validation requirements.
Create and manage project plans including schedules, budgets, and stakeholder updates.
Develop documentation for equipment including specifications, assembly instructions, maintenance, and calibration procedures.
Create and execute protocol documentation for equipment DQ, IQ, OQ, PQ validations.
Conduct effective design reviews of new equipment at all stages of development.
Provide equipment-related technical support for on-going production operation and expansion.
Establish and manage external resources (contractors, system integrators, vendors) in the planning and execution of equipment projects including duplication activities.
Support other equipment-related operations and duties as required
Qualifications:
Required Skills and Experience
Minimum BSME or similar.
Minimum 3 years' experience designing and developing Automated manufacturing equipment.
Self-motivated, works well with others in a team environment.
Proficiency with CAD (SolidWorks highly preferred): designing parts with complex geometry, creating assemblies and creating detailed manufacturing drawings
Comfortable operating machine shop, measurement, and test equipment
Mechanical design and exploration skills, including statics, dynamics, and strength of materials, including stress analysis, fatigue, and thermal
Experience in integration of mechatronics components such as sensors, motors, pneumatics, and motion and vision control components.
Experience troubleshooting and repairing manufacturing equipment.
Experience developing equipment qualification, calibration and PM procedures and practices.
Required Education and Training
Minimum BSME Mechanical or Mechatronics engineering with a minimum of 5 years’ related experience.
Experience with enterprise software (e.g. Agile document control, Confluence, Polarion, Windchill, etc)
Prior experience working with PLM systems (Agile preferred), SAP applications, including ECO creation, origination of equipment specification, test protocols, BOM, and work instructions.
Preferred Skills and Experience:
Excellent understanding of tolerance analysis and statistical methods. Fluency in ASME Y14.5 GD&T and tolerance stack analysis
MSME (or equivalent) with a minimum of 6 plus years’ prior experience.
Structured Problem Solving. Rational thinking and root cause analysis capability.
Experience working in a medical device or other regulated quality systems.
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