TOPPAN Packaging Americas
Overview
TEQ, a division of Toppan, is a leading provider of innovative thermoformed packaging solutions for the healthcare and medical device industries. We design and produce medical devices, sterile barrier systems, medical trays, and other critical packaging that meets the highest standards of safety, compliance, and performance. With a commitment to sustainability, regulatory excellence, and customer collaboration, TEQ delivers packaging that protects, performs, and enhances patient outcomes. 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. Evaluate and select materials aligned with performance, sterilization compatibility, sustainability, and cost objectives. Conduct feasibility studies including draft analysis, stackability, and functional integrity of sterile packaging systems. Collaborate closely with Tool Design Engineering and production teams to ensure designs are practical, efficient, and manufacturable. Work with quality and regulatory teams to ensure compliance with FDA, ISO 13485, and GMP requirements. Support packaging validation activities, including sample production, functional testing, and documentation for IQ/OQ/PQ. Participate in customer and internal meetings to understand needs, present design concepts, and refine solutions. Identify potential design, material, or process risks early in the project lifecycle, and proactively develop mitigation strategies. Maintain accurate design documentation and manage revisions through PDM/PLM systems. Stay current with materials, sterilization methods (EtO, gamma, e-beam), design trends, and technologies relevant to medical packaging. Qualifications
Bachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Design, or related field. 2+ years of experience in packaging design, with a strong preference for medical device packaging. Proficiency with 3D CAD software (SolidWorks strongly preferred). Strong knowledge of thin-gauge thermoformed packaging design, including draft angles, wall thickness, and undercuts. Understanding of material properties relevant to PETG, HIPS, PP, or similar plastics used in sterile barrier systems. Familiarity with production tooling processes and ability to integrate packaging design considerations with tooling and manufacturing requirements. Knowledge of FDA, ISO 11607, ASTM, and ISO 13485 standards for medical packaging. Ability to identify risks during design and commercialization phases and develop effective mitigation strategies. Excellent problem-solving and communication skills with attention to both functionality and usability. Ability to manage multiple projects and meet deadlines in a regulated, dynamic environment. Experience designing thermoformed trays, sterile barrier systems, or pharmaceutical packaging. Familiarity with packaging validation protocols (IQ/OQ/PQ) and documentation practices. Experience with cleanroom manufacturing and regulatory audits. Understanding of human factors and usability in medical packaging design. Location & Employment
This position is an onsite role at our Huntley, IL facility. Employment type:
Full-time Seniority level:
Mid-Senior level Note:
This description reflects the responsibilities and qualifications for the role as posted. The company reserves the right to modify requirements or responsibilities at any time.
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TEQ, a division of Toppan, is a leading provider of innovative thermoformed packaging solutions for the healthcare and medical device industries. We design and produce medical devices, sterile barrier systems, medical trays, and other critical packaging that meets the highest standards of safety, compliance, and performance. With a commitment to sustainability, regulatory excellence, and customer collaboration, TEQ delivers packaging that protects, performs, and enhances patient outcomes. 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. Evaluate and select materials aligned with performance, sterilization compatibility, sustainability, and cost objectives. Conduct feasibility studies including draft analysis, stackability, and functional integrity of sterile packaging systems. Collaborate closely with Tool Design Engineering and production teams to ensure designs are practical, efficient, and manufacturable. Work with quality and regulatory teams to ensure compliance with FDA, ISO 13485, and GMP requirements. Support packaging validation activities, including sample production, functional testing, and documentation for IQ/OQ/PQ. Participate in customer and internal meetings to understand needs, present design concepts, and refine solutions. Identify potential design, material, or process risks early in the project lifecycle, and proactively develop mitigation strategies. Maintain accurate design documentation and manage revisions through PDM/PLM systems. Stay current with materials, sterilization methods (EtO, gamma, e-beam), design trends, and technologies relevant to medical packaging. Qualifications
Bachelor’s degree in Packaging Engineering, Mechanical Engineering, Industrial Design, or related field. 2+ years of experience in packaging design, with a strong preference for medical device packaging. Proficiency with 3D CAD software (SolidWorks strongly preferred). Strong knowledge of thin-gauge thermoformed packaging design, including draft angles, wall thickness, and undercuts. Understanding of material properties relevant to PETG, HIPS, PP, or similar plastics used in sterile barrier systems. Familiarity with production tooling processes and ability to integrate packaging design considerations with tooling and manufacturing requirements. Knowledge of FDA, ISO 11607, ASTM, and ISO 13485 standards for medical packaging. Ability to identify risks during design and commercialization phases and develop effective mitigation strategies. Excellent problem-solving and communication skills with attention to both functionality and usability. Ability to manage multiple projects and meet deadlines in a regulated, dynamic environment. Experience designing thermoformed trays, sterile barrier systems, or pharmaceutical packaging. Familiarity with packaging validation protocols (IQ/OQ/PQ) and documentation practices. Experience with cleanroom manufacturing and regulatory audits. Understanding of human factors and usability in medical packaging design. Location & Employment
This position is an onsite role at our Huntley, IL facility. Employment type:
Full-time Seniority level:
Mid-Senior level Note:
This description reflects the responsibilities and qualifications for the role as posted. The company reserves the right to modify requirements or responsibilities at any time.
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