Mechanical Engineer (Contractor)
About The Position
Vantage MedTech provides comprehensive design and manufacturing services, supporting the advancement of medical technologies from concept through to product realization. We develop and manufacture new products for the treatment of heart failure, cancer, stroke, Gene Therapy, COPD, TBI, Atrial Fibrillation, Blood Clots, Brain Surgery, and many more! We are searching for top-tier talent to apply their gifts to making life better for hundreds of thousands of patients worldwide. If this is something you aspire to, we would like to talk with you! This is an independent contractor role for a defined term of approximately 12 months, with potential for extension. This role is not an employee position and is not eligible for company sponsored benefits.
Requirements
- Bachelor’s degree in mechanical engineering or a related field
- 5+ years of industry experience in the design, development, and testing of mechanical systems
- Intermediate to advanced proficiency in CAD modeling (SolidWorks preferred), including advanced part, surfacing, and parametric feature modeling
- Demonstrated ability to create detailed engineering drawing packages with proper dimensioning and tolerancing for moderately to highly complex assemblies
- Strong understanding of GD&T and tolerance stack-up analysis
- Experience applying Design for Manufacturability (DFM), Design for Assembly (DFA), and cost optimization principles, along with knowledge of manufacturing methods and production processes
- Experience performing static structural finite element analysis (FEA/FEM)
- Ability to develop design input requirements for complex mechanical systems and components
- Working knowledge of medical and mechanical safety standards and the ability to design for compliance
- Experience with rapid prototyping, including 3D printing and model fabrication for usability testing
- Ability to interact effectively with clients.
- Excellent critical thinking and analytical skills.
- High level of initiative with ability to self-manage.
- Strong written and verbal communication skills as well as reporting and presentational skills.
- All applicants must be authorized to perform services in the United States without sponsorship.
Nice To Haves
- Familiarity with CFD for simple fluidic systems, as well as heat transfer and fluid flow analysis
- Experience leading or contributing to mechanical hazard analyses and product/hardware FMEA activities
- Experience working within a regulated quality system (e.g., ISO 13485)
- Familiarity with biocompatibility considerations and ISO 10993-1 compliance
- Understanding of sterilization methods and ability to evaluate material compatibility and effects
- Regulatory agency experience including UL, CE and FDA approval processes
Responsibilities
- Designing and developing mechanical components and systems for medical devices in alignment with applicable regulatory standards (ISO 13485, FDA, MDR)
- Creating and maintaining engineering documentation, including CAD models, drawings, tolerance analyses, and material specifications
- Collaborating with cross-functional stakeholders to support design, integration, and system-level problem solving
- Supporting design transfer activities, including supplier coordination, Design for Manufacturability (DFM), and Design for Assembly (DFA)
- Delivering engineering analyses and technical outputs with a high degree of autonomy and professional judgment
- Investigate clinical requirements.
Benefits
- This role is not an employee position and is not eligible for company sponsored benefits.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
