Design Engineer

Position Overview

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions.

The Design Engineer I/II at Applied Medical is responsible for developing and refining innovative medical devices and its processes that improve patient outcomes and advance minimally invasive surgery. This hands-on role involves designing, prototyping, and testing components, assemblies and equipment within a collaborative engineering environment. Based onsite at Applied Medical’s global headquarters, the Design Engineer I/II (also referred to as an Engineer I/II) works closely with manufacturing, quality, and clinical teams to transform design concepts into high-quality, manufacturable products.

Key Responsibilities

• Design and develop medical device components, assemblies, and fixtures using Computer-Aided Design (CAD) tools such as SolidWorks.
• Build and test prototypes to evaluate design feasibility, functionality, and manufacturability.
• Collaborate with cross-functional teams, including manufacturing, clinical development, and quality engineering, to ensure product design alignment across the full development cycle.
• Prepare detailed design documentation, including engineering drawings, models, and design review materials.
• Apply Geometric Dimensioning and Tolerancing (GD&T) to ensure precision in component and assembly designs.
• Conduct product verification and validation testing, documenting results and implementing design improvements.
• Conduct design analyses and participate in risk assessments to ensure compliance with medical device regulations and standards.
• Participate in process development to ensure seamless transition from design to production.
• Add about machine/equipment troubleshooting and documentation.

Required Qualifications

• Education: Bachelor’s degree in mechanical, industrial, or manufacturing engineering, or equivalent.
• Experience Required: Up to two years of relevant engineering experience in product design, prototyping, or process development.
• Proficiency with CAD software such as SolidWorks for 2D and 3D modeling.
• Understanding of GD&T and engineering documentation standards.
• Experience creating and testing prototypes using hands-on tools and fabrication techniques.
• Strong analytical and technical problem-solving skills.
• Excellent communication, organization, and documentation abilities.
• Ability to work collaboratively in cross-functional teams and operate independently when required.

Preferred Qualifications

• Experience in medical device design, manufacturing, or regulated industry environments.
• Knowledge of surgical procedures, minimally invasive technologies, or clinical applications.
• Familiarity with FDA and ISO 13485 quality systems and design controls.
• Exposure to Failure Mode and Effects Analysis (FMEA) and Test Method Validation (TMV).
• Experience with Finite Element Analysis (FEA), tolerance analysis, or statistical analysis using Minitab.
• Working knowledge of Product Lifecycle Management (PLM) systems such as NetWeaver.

Benefits & Perks

• Compensation: $71,000 - $95,000 per year (California).
• Benefits: Comprehensive benefits package.
• Training and mentorship opportunities.
• On-campus wellness activities.
• Education reimbursement program.
• 401(k) program with discretionary employer match.
• Generous vacation accrual and paid holiday schedule.