Job Description:
The CAD Design Specialist II (CAD II) is responsible for converting client data into customized prosthetic device designs using various software tools. Additionally, this position is responsible for the design review process within the production design team. This role also entails troubleshooting issues related to the design process, providing mentorship to CAD Design Specialist I, and maintaining design templates. Additionally, CAD II is responsible for documenting procedures and participating in continuous improvement projects as assigned.
Responsibilities:
Mentor team members by assisting in problem-solving and troubleshooting.
Apply proven product knowledge to candidacy assessment and revision cases by assessing clinical information provided in video, images, and/or other various media.
Audit completed custom design files and release to production.
Provide design training to CAD Design Specialist I as directed by the Manager.
Work autonomously to successfully complete projects in collaboration with both the R&D and Manufacturing teams as assigned.
Work independently to achieve assigned objectives.
Design in various software environments to create custom-fit prosthetic device designs and design revisions.
Use calibrated tools to collect measurements from physical casts or utilize CAD software to analyze digital scans and/or scale digital images.
Analyze client data and collaborate with clinical experts to establish a design framework.
Generate design documentation and communicate considerations for customer-facing departments.
Work closely with in-house clinical experts to evaluate the fit of devices on the end-user. Implement and recommend modifications to existing designs as needed.
Transfer CAD design files to ERP software, manage the bill of materials, and work closely with the manufacturing team to ensure that the product aligns with the design.
Collaborate with stakeholders to troubleshoot production-related challenges related to custom product design and recommend solutions.
Adhere to established requirements and procedures within the Quality Management System (QMS)
Build relationships with key stakeholders to establish trust and credibility as a design professional.
Exercise good use of company funds and property within the set guidelines. Always maintains an honest and professional attitude as the company’s representative.
Contribute to a safe working environment by maintaining own workspace and reporting any potential hazards.
Qualifications:
Vocation certification or an Associate’s degree
Minimum of 3 years of relevant experience
Experience in 3D CAD design systems, preferably SolidWorks
Experience with Microsoft Office
Demonstrated knowledge of prosthetic design principles
Experience in a manufacturing environment.
Familiarity with GD&T drawing standards
Össur is a leading global provider of prosthetics and bracing and supports solutions.
Embla Medical is an equal opportunity employer and makes employment decisions on the basis of merit. We want to have the best available individual in every job.
Embla Medical's equal opportunity policy prohibits all discrimination (based on race, color, creed, sex, religion, marital status, age, national origin or ancestry, physical disability, mental disability, military service, pregnancy, child birth or related medical condition, actual or perceived sexual orientation, or any other consideration made unlawful by local laws around the world).
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