Location: Danvers, MA
Minimum Qualifications
• BS degree in relevant discipline (mechanical or electrical engineering or applied physics) with 5+ year of experience in product design (concept generation, detailed design), fixture development and testing.
• Knowledge on mechanical engineering drawing principles.
• Good in communication
• Good exposure in Medical Device product development process.
• Shall work independently
Preferred Qualifications
• Support in design, development, improvement of Test fixtures to meet the requirements for new and existing products Manufacturing and Testing.
• Support Test method validations in qualifying the Equipment / Tooling / Fixtures.
• Support CAD activities, CR Review of 3D CAD models and 2D drawings for CR release.
• Participate in generating innovative concepts and system layouts in 3D CAD for Test Fixture and Automation tools.
• Support in Mockup and prototyping of new products for proof-of-concept evaluation.
• Collaborate with supplier for development of Tools and fixtures to improve product robustness and manufacturability.
• Support in Fixture rework, Assembly, Test Setup, and preliminary testing activities.
• Co-ordinate with Vendors for Quote, PO, Fixture fabrication, Inspection and follow up.
• Ensure project status, schedule progress and key project metrics to senior management.
• Responsible for or more of the following:
o In a supervisory capacity, plans, develops, coordinates, and directs a large important engineering project or several small projects with many complex features.
o As an individual researcher, carries out complex or novel assignments requiring the development of new or improved techniques or procedures.
o Work is expected to result in the development of new or improved techniques or procedures.
o Work is expected to result in the development of new or refined equipment, materials, processes, products, and/or methods.
Required Knowledge, Skills
• English communication skills, written and oral.
• Must be proficient in reading Drawings and CAD
• Must be able to demonstrate a proven track record of leading design work and proving feasibility for manufacturing transfer of design.
• Medical device design experience is a plus or similar work within a regulated industry.
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