Job Description
We are seeking a skilled CAD Specialist to develop and modify 3D models, drawings, and technical documentation using CAD software such as UG NX, Creo, or SolidWorks. This role involves ensuring design accuracy and compliance with medical device industry standards and regulatory requirements. The CAD Specialist will collaborate with engineering teams to support product development, prototyping, and manufacturing, managing design revisions and maintaining design history files in accordance with engineering change management procedures. Additionally, the role includes utilizing PLM systems for version control, documentation, and workflow coordination, assisting in design feasibility assessments and optimization for manufacturability, conducting tolerance analysis, and supporting design verification activities.
ResponsibilitiesDevelop and modify 3D models, drawings, and technical documentation using CAD software.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 SkillsProficiency in CAD tools like UG NX, Creo, or SolidWorks.Familiarity with PLM systems.Basic understanding of engineering change management processes.Additional Skills & QualificationsExperience in the medical device industry is preferred.Knowledge of industry regulations such as ISO and FDA is advantageous.Work Environment
The work environment is onsite, providing a collaborative setting with engineering and quality assurance teams. Enjoy 2 weeks of PTO and 10 paid holidays annually. The position requires adherence to industry standards and regulatory compliance, with a focus on design precision and manufacturability optimization.
Pay and Benefits
The pay range for this position is $42.00 - $47.00/hr.
Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Irvine,CA.
Application Deadline
This position is anticipated to close on May 30, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.