Design Engineers – R&D (2 postes ouverts)
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Location: Chicago Area (On-site – 100%)
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Start Date: ASAP
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Position Overview
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We are seeking two Design Engineers to support R&D project teams at our client's Chicago-area site, working on drug delivery device components and assembly systems. We're hiring for two distinct focus areas — please indicate which profile best matches your background when applying.
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Profile 1 – Mechanical Design & Prototyping
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Contributes to the design and development of mechanical components and assemblies, working closely with engineering, prototyping, and manufacturing teams.
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Key Responsibilities
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- Design and develop mechanical components and assemblies for medical device products using SolidWorks.
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- Support R&D development activities from concept through prototyping and testing.
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- Collaborate with engineering and manufacturing teams on assembly line design and optimization.
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- Create and update 3D models, drawings, and technical documentation.
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- Participate in prototyping activities, including 3D printing and early-stage product iterations.
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- Contribute to design verification and testing activities.
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- Support data analysis related to design performance and testing results when required.
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Qualifications
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- Bachelor's or Master's degree in Mechanical Engineering or related field.
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- Around 5 years of experience in mechanical design or product development.
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- Experience with SolidWorks CAD software.
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- Solid knowledge of mechanical design principles.
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- Experience with plastic components or plastics processing is a strong advantage.
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- Exposure to assembly lines or manufacturing environments is preferred.
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- Experience with 3D printing / rapid prototyping is a plus.
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- Experience preparing or supporting technical documentation (design records, drawings, specifications) is a plus.
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Profile 2 – Design Control & Verification
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Focused on design control documentation, process compliance, and test method development rather than hands-on CAD or tolerance analysis. Requires building a solid understanding of the device and how it functions to support documentation and verification activities.
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Key Responsibilities
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- Support and maintain design control documentation throughout the product development lifecycle.
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- Ensure project activities align with and follow the established development process.
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- Develop, plan, and execute mechanical test methods in support of design verification.
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- Support validation activities and design verification planning.
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- Work closely with engineering teams to understand device functionality and translate it into clear documentation.
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- Track and support non-technical/process-oriented deliverables to keep the project on track.
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- Collaborate with cross-functional teams (engineering, quality, manufacturing) to ensure documentation accuracy and completeness.
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Qualifications
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- Bachelor's or Master's degree in Mechanical Engineering or related field.
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- Around 5 years of experience in mechanical design or product development.
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- Strong experience in mechanical test method development, validation, and design verification planning and execution.
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- Solid understanding of design control processes within a medical device or regulated environment.
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- Experience with drug delivery or injection devices is a strong plus.
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- Comfortable working on documentation-heavy, process-driven tasks rather than deep technical/CAD work.
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- Strong organizational skills and attention to detail.
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Additional Requirements (both profiles)
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- Ability to work on-site in the Chicago area.
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- Comfortable working in a fast-paced R&D environment.
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- Availability to start immediately (ASAP).
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