Sr. Mechanical Engineer - Andover, United States - Softworld, a Kelly Company

Description

Job Title

:

Sr. Mechanical Engineer
Location

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Andover MA 01810

Onsite Requirements :

Injection Molding
Product Development
Medical Device
Job Description
:

ESSENTIAL TASKS/ DUTIES INCLUDE

:

Responsible for CAD design, building, and testing of new concepts and iterating through the design process.
Provide direction to engineers, technicians, external industrial design teams, and OEM manufacturers.

Work closely with manufacturing engineering and apply DFM techniques to ensure product is capable of being assembled and tested using automation.

Perform thorough analysis (tolerance, dFMEA, DOE, statistical) to ensure product will meet design requirements.
Manage injection mold suppliers through the tool development process and ensure conformance to specifications.
Develop drawings and release documentation in accordance with applicable standards and SOPs.
Assist V&V testing with protocols, reports, fixtures, and TMVs.
Maintain DHF including design reviews, reports, meeting minutes, etc.
Perform other development tasks and duties as required.


BACKGROUND AND QUALIFICATIONS
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8 years of product development experience as mechanical design engineer with 3 years in a lead role for complex Class II or III disposables and electromechanical medical equipment.

Expert in Solidworks 3D modeling and design. 3D surfacing expertise desired.
Experienced in design of injection molded disposables and plastic joining techniques including ultrasonic/RF/laser welding and adhesive/solvent bonding.
Some experience in design of electromechanical sub-systems including machined/sheet metal components and motorized assemblies.

Solid foundation of mechanical engineering fundamentals and ability to perform engineering analysis including tolerance analysis, GD&T, FEA, engineering 1st principles.

Ability to work independently with some guidance.

Must be a creative problem solver that can think outside of the box to develop novel solutions to complex problems.

Hands-on skills and ability to use power tools and light machine shop equipment required.
Strong written and verbal communication skills are required.
Understanding of medical device development processes including experience with FDA CFR 820, ISO 13485, IEC regulations and standards.

Must be able to work in a fast paced, high energy, collaborative team that possesses a strong sense of urgency.

Project management experience & Six Sigma Green Belt desired.
Ability to be onsite 5 days per week and lift 25lbs.
5% Domestic or International travel may be required.


EDUCATION
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BS in Mechanical Engineering, Plastics Engineering, Biomedical Engineering, or equivalent is required.

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