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Cad Specialist

Actalent

Posted Saturday, June 7, 2025

Posting ID: JP-005333434

Irvine, CA
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Job Title: CAD Specialist

For immediate consideration, please apply directly to this job posting AND email me at biacosta @actalentservices.com with the following:

1) Word copy of resume

2) 2-3 professional references

3) 4-5 brief bullet points highlighting technical qualifications


Job Description

As a CAD Specialist, you will be responsible for developing and modifying 3D models, drawings, and technical documentation using CAD software such as UG NX, Creo, or SolidWorks. You will ensure design accuracy and compliance with medical device industry standards and regulatory requirements. Collaboration with engineering teams will be essential to support product development, prototyping, and manufacturing processes.


Responsibilities

  • Develop and modify 3D models, drawings, and technical documentation using CAD software (UG NX, Creo, or SolidWorks).
  • Ensure design accuracy and compliance with medical device industry standards and regulatory requirements.
  • Collaborate with engineering teams to support product development, prototyping, and manufacturing.
  • Manage design revisions and maintain design history files in accordance with engineering change management procedures.
  • Utilize PLM systems for version control, documentation, and workflow coordination.
  • Assist in design feasibility assessments and optimization for manufacturability.
  • Conduct tolerance analysis and support design verification activities.
  • Work closely with quality assurance teams to align designs with industry regulations (ISO, FDA).

Essential Skills

  • Proficiency in CAD tools like UG NX, Creo, or SolidWorks.
  • Familiarity with PLM systems.
  • Basic understanding of engineering change management processes.
  • Experience with mechanical design and CAD in the medical device industry.

Additional Skills & Qualifications

  • Experience in design feasibility assessments.
  • Knowledge of design verification and tolerance analysis.
  • Ability to work closely with quality assurance teams.
  • Understanding of industry regulations (ISO, FDA).

Work Environment

This position is onsite, offering 2 weeks of PTO and 10 paid holidays. You will be working in a collaborative environment, utilizing advanced technologies and equipment to ensure high standards in product development and manufacturing processes.

Compensation:$47

Contact Information

Recruiter: Bianca Acosta

Phone: +15625664747

Email: biacosta@actalentservices.com

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
On-Site
Workflow Management
New Product Development
Version Control
Manufacturing Processes
Change Management
Prototyping
3D Modeling
Computer-Aided Design
Product Lifecycle Management
Quality Assurance
Medical Devices
Technical Documentation
Mechanical Design
Design Verification
Tolerance Analysis
Engineering Tolerance
PTC Creo (CAD Suite)
SolidWorks (CAD)
Industry Standards

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