Gentis Solutions

CAD Administrator / Design Engineer

Apply Now
Wilmington, OH
90k/year - 100k/year
January 16, 2025
Applicants: 0 Interviewing: 2 Hired: 0
Direct Hire In Person
Rob Redmond

Rob Redmond

Director of Sales
Engineering Aerospace Architecture

About the Job

Gentis Solutions is looking for a CAD Administrator / Design Engineer to join our client's team. Client-specific benefits are available and will be discussed in detail during your interview.

Compensation for this position ranges from 90k/year - 100k/year per year, based on experience. Payment is bi-weekly and is based on all hours worked, without eligibility for overtime.

This position requires the individual to be located in the Wilmington, OH area.

Requirements

Education and Experience

  • Bachelor’s degree in Engineering (Mechanical, Electrical, Biomedical, or related discipline).

  • Minimum of 10 years of experience with SolidWorks (CSWE certification preferred).

  • Minimum of 10 years of experience with SolidWorks PDM (CPAP certification preferred).

  • Experience in CAD administration, including global onboarding, troubleshooting, and maintenance.

  • Experience in managing Global PDM Vaults and workflows.

  • Proven ability to develop and sustain new and existing products.

  • Experience with BOM structuring, modeling configurations, and creating assembly drawings with 500+ components.

  • Proficiency in producing technical documentation, procedures, and instructions for process control.

  • Ability to work effectively across multiple time zones, including occasional evenings and weekends. Technical Skills

  • Proficiency in interfacing compatibilities between SolidWorks and Altium Designer, and SolidWorks PDM and ERP systems.

  • Ability to manage file permissions, execute part number creation processes, and assist with IT upgrades globally.

  • Expertise in material selection, CAD renderings, and SolidWorks Simulation. Industry Knowledge

  • Exposure to medical devices and/or ISO 13485 standards.

  • Experience with FDA, ISO 13485, ISO 14971, MDD 93/42/EEC, and MDR compliant product design or redesign.

  • Familiarity with Engineering Change Order and/or Phase-Gate processes to ensure QMS compliance. 

Nice-to-Have Skills

CAD Administration

  • Experience with SolidWorks Composer and CAMWorks.

  • Familiarity with onboarding new ERP systems.

  • Experience hosting executable files on collaborative drives and managing file structuring and rollback processes. Design Engineering

  • Ability to create dummy models for external final stage partners (e.g., ambulance builders).

  • Proficiency in creating marketing-oriented CAD renderings.

  • Experience with electro-mechanical and hydraulic device design.

  • Exposure to electrical assemblies and wiring diagram creation. Industry and Compliance

  • Familiarity with ISO standards related to medical devices (ISO 13485, ISO 14971).

  • Experience designing FDA and MDR-compliant products. Other Skills

  • Experience with medical device development.

  • Exposure to SolidWorks Simulation for product analysis and optimization.