Medical Packaging Design Engineer — Onsite in Huntley, IL

ESPO Corporation; Huntley (IL); On-site; USD 85,000 - 100,000; Full time

Benefits offered by this job

PTO

Health and dental insurance

401k

Job summary

ESPO Corporation is seeking a Packaging Design Engineer to lead the design and development of thermoformed medical packaging products in Huntley, IL. The role focuses on translating customer requirements into manufacturable, compliant, and high-performance sterile packaging solutions.

You will use SolidWorks for 3D CAD modeling, drive design validation, and collaborate with quality and regulatory teams to ensure FDA/ISO 13485/GMP compliance.

Qualifications

• Bachelor's degree in packaging, mechanical, or industrial design.
• 2+ years of experience in packaging design, preferably medical device packaging.
• Proficiency with SolidWorks CAD software.

Responsibilities

• Design thermoformed sterile packaging products from concept through production using CAD software (e.g., SolidWorks).
• Translate customer and regulatory specifications into innovative, compliant packaging designs.
• Develop detailed 3D models, assemblies, and 2D drawings for medical packaging products.
• Utilize 3D scanning and 3D printing technologies to support prototype development, design validation, and rapid iteration.
• Collaborate with quality, regulatory, and production teams to ensure compliance and manufacturability.
• Maintain design documentation and manage revisions through PLM systems.

Skills

Design integration

Regulatory awareness

Cross-functional collaboration

Education

Bachelor's degree in Packaging Eng./Mech./Industrial Design

Tools

SolidWorks

PDM/PLM

3D scanning

3D printing

Job description

ESPO Corporation is seeking a Packaging Design Engineer to lead the design and development of thermoformed medical packaging products in Huntley, IL. The role focuses on translating customer requirements into manufacturable, compliant, and high-performance sterile packaging solutions.

You will use SolidWorks for 3D CAD modeling, drive design validation, and collaborate with quality and regulatory teams to ensure FDA/ISO 13485/GMP compliance.