Sr. Mechanical Engineer
Found in: Appcast Linkedin GBL C2 - 2 weeks ago
Job Title: Sr. Mechanical Engineer
Location: 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:
- 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 60601-1 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:
- BS in Mechanical Engineering, Plastics Engineering, Biomedical Engineering, or equivalent is required.
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