Design Support Engineer

Date Posted: 08/27/2025

Hiring Organization: Rose International

Position Number: 487696

Industry: Biotech

Job Title: Design Support Engineer

Job Location: Indianola, PA, USA, 15051

Work Model: Hybrid

Work Model Details: Onsite 2-3 days/week

Shift: Normal business hours

Employment Type: Temporary

FT/PT: Full-Time

Estimated Duration (In months): 13

Min Hourly Rate($): 50.00

Max Hourly Rate($): 70.00

Must Have Skills/Attributes: 2D, 3D, AutoCAD, Creo, Drafting, Medical device, Solidworks

Experience Desired: Experience in the medical field industry (12 yrs)

Required Minimum Education: Associate’s Degree

Preferred Education: Bachelor’s Degree

**C2C is not available**

Job Description
Education Requirements:

• Minimum of an Associate’s degree in a technical field.

Required Skills for the Design Support Engineer:

• Strong proficiency in Pro/Engineer/Creo, Solidworks, and AutoCAD for assemblies, component, and drawing designs.
• Comprehensive knowledge of detail drafting practices with the ability to create/update drawings using GD&T practices.
• Strong analytical abilities with a strategic approach to resolving issues.
• Effective verbal and written communication skills.
• Ability to navigate change and ambiguity while considering different organizational perspectives.
• Minimum of 12 years full-time relevant experience within the medical device industry.
• Familiarity with applicable standards related to medical devices.
• Some familiarity with Regulatory, Quality, Procurement, and Risk Management processes.

Design Support Engineer Overview:
In this role, you will play a crucial part in the design process within the Radiology Life Cycle Engineering team, contributing to the maintenance and enhancement of existing product lines for sterile disposables and electro-mechanical components used in medical imaging. You will provide CAD design support, troubleshoot design issues, and ensure compliance with engineering standards throughout the product lifecycle. Your expertise will be essential in collaborating with engineers and stakeholders to deliver high-quality design documentation and support innovative solutions in the medical device industry.

Responsibilities:

• Work with lead engineers to maintain 2D and 3D CAD assembly and part models, as well as drawings for electro-mechanical and sterile disposable products.
• Rigorously maintain CAD design documents to company standards, ensuring accurate detailed design packages.
• Assist engineers in troubleshooting design or model issues, including remodeling or restructuring as necessary.
• Prepare engineering drawings in compliance with company and engineering standards, including Geometric Dimensioning and Tolerancing (GD&T).
• Collaborate on engineering CAD/drawing release and change documentation via PTC Windchill Product Data Management system.
• Support staff members to complete work and projects accurately and timely.
• Apply good modeling techniques to update existing models and develop new concept models for components and subsystems.
• Provide full lifecycle engineering support for product designs utilized in radiology and cardiovascular medical procedures.
• Maintain mechanical designs related to injection molding, machining, extrusion, assembly, and labeling.
• Research and develop new technologies associated with medical products.
• Author and maintain detailed product requirements and design outputs.
• Maintain design history file documentation throughout the product development process.
• Lead small teams on lower complexity project activities and participate in design reviews as a reviewer.
• Write scientific protocols, manage execution of protocols, analyze results, and write reports.
• Interface with authorities and auditors regarding product design-related topics.
• Collaborate with stakeholders to initiate and execute projects effectively while delivering maximum value.
• Communicate effectively with a diverse range of internal and external stakeholders.

• **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

• **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**

Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations’ website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).