Partner closely with medical device clients and internal teams (marketing, product management, quality, operations) to align development with customer needs and ensure successful product integration.
Partner closely with medical device clients and internal teams (marketing, product management, quality, operations) to align development with customer needs and ensure successful product integration.
Product Design Engineer, IoT
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
Madison, WI · On-site
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
Madison, WI · On-site
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
Madison, WI · On-site
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Product Design Engineer, IoT
Madison, WI · On-site
$130K - $156K/yr
... and other medical device documentation processes as required by Quality Management System (QMS). 6. Interest in future integration of automation or AI-enhanced tools in engineering workflows.
Senior Sustaining Engineer - Electrical
$108K - $141K/yr
Strong understanding of cGMP, ISO 13485, and regulated medical device environments * Experience ... integration. * Proficiency in analog and digital circuit design, analysis, and simulation.
Senior Sustaining Engineer - Electrical
$108K - $141K/yr
Strong understanding of cGMP, ISO 13485, and regulated medical device environments * Experience ... integration. * Proficiency in analog and digital circuit design, analysis, and simulation.
Senior Sustaining Engineer - Electrical
Madison, WI · On-site
$108K - $141K/yr
Strong understanding of cGMP, ISO 13485, and regulated medical device environments * Experience ... integration. * Proficiency in analog and digital circuit design, analysis, and simulation.
Senior Sustaining Engineer - Electrical
Madison, WI · On-site
$108K - $141K/yr
Strong understanding of cGMP, ISO 13485, and regulated medical device environments * Experience ... integration. * Proficiency in analog and digital circuit design, analysis, and simulation.
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$90 - $120/hr
... medical device design-control expectations. Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$90 - $120/hr
... medical device design-control expectations. Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$131K - $173K/yr
... medical device design-control expectations. * Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$131K - $173K/yr
... medical device design-control expectations. * Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$131K - $173K/yr
... medical device design-control expectations. * Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$131K - $173K/yr
... medical device design-control expectations. * Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$131K - $173K/yr
... medical device design-control expectations. * Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Software Engineer - Embedded Platform
Waukesha, WI · On-site
$131K - $173K/yr
... medical device design-control expectations. * Participate in technical design reviews, code reviews, integration reviews, risk-based engineering discussions, static analysis, unit testing, and ...
Fullstack Engineer
Madison, WI · On-site
The Software engineer collaborates in a complex environment integrating software with other software and hardware subsystems for an advanced medical device. Our work has a daily impact on patients ...
Fullstack Engineer
Madison, WI · On-site
The Software engineer collaborates in a complex environment integrating software with other software and hardware subsystems for an advanced medical device. Our work has a daily impact on patients ...
Fullstack Engineer
Madison, WI · On-site
The Software engineer collaborates in a complex environment integrating software with other software and hardware subsystems for an advanced medical device. Our work has a daily impact on patients ...
Fullstack Engineer
Madison, WI · On-site
The Software engineer collaborates in a complex environment integrating software with other software and hardware subsystems for an advanced medical device. Our work has a daily impact on patients ...
Fullstack Engineer
Madison, WI · On-site
The Software engineer collaborates in a complex environment integrating software with other software and hardware subsystems for an advanced medical device. Our work has a daily impact on patients ...
Fullstack Engineer
Madison, WI · On-site
The Software engineer collaborates in a complex environment integrating software with other software and hardware subsystems for an advanced medical device. Our work has a daily impact on patients ...
Product Manager EMG
Middleton, WI · On-site +1
$120K - $130K/yr
... through a comprehensive approach that integrates product specifications, clinical data ... healthcare/medical device industry • Demonstrated success in product launches and ...
Product Manager EMG
Middleton, WI · On-site +1
$120K - $130K/yr
... through a comprehensive approach that integrates product specifications, clinical data ... healthcare/medical device industry • Demonstrated success in product launches and ...
Product Manager PSG
Middleton, WI · On-site
$100K - $110K/yr
Translate market needs into successful product launches by integrating product specifications ... Experience with regulatory compliance within the healthcare/medical device industry . Skills ...
Product Manager PSG
Middleton, WI · On-site
$100K - $110K/yr
Translate market needs into successful product launches by integrating product specifications ... Experience with regulatory compliance within the healthcare/medical device industry . Skills ...
Engineering Manager
Kenosha, WI · On-site
$110K - $130K/yr
New Product Integration * Collaborate with R&D and product development teams to ensure smooth ... Knowledge of materials, tooling, and medical device manufacturing processes. * Strong understanding ...
Engineering Manager
Kenosha, WI · On-site
$110K - $130K/yr
New Product Integration * Collaborate with R&D and product development teams to ensure smooth ... Knowledge of materials, tooling, and medical device manufacturing processes. * Strong understanding ...
Fully integrate into NorthStar's mission to revolutionize oncology treatment by providing patients ... medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial ...
Fully integrate into NorthStar's mission to revolutionize oncology treatment by providing patients ... medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial ...
Radiopharmaceutical Manufacturing Specialist (1st shift)
Beloit, WI · On-site
$27.50/hr
Fully integrate into NorthStar's mission to revolutionize oncology treatment by providing patients ... medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial ...
Radiopharmaceutical Manufacturing Specialist (1st shift)
Beloit, WI · On-site
$27.50/hr
Fully integrate into NorthStar's mission to revolutionize oncology treatment by providing patients ... medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial ...
Fully integrate into NorthStar's mission to revolutionize oncology treatment by providing patients ... medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial ...
Fully integrate into NorthStar's mission to revolutionize oncology treatment by providing patients ... medical device), ISO 15189 (hospital), CLIA (clinical laboratory), ISO 9001 (industrial ...
Medical Device Integration information
What is a medical device integration?
A Medical Device Integration job involves connecting medical devices to healthcare IT systems, such as electronic health records (EHRs), to ensure seamless data exchange. Professionals in this role configure, test, and troubleshoot interfaces between devices and software to improve clinical workflows and patient care. They work closely with biomedical engineers, IT specialists, and healthcare providers to ensure reliable and accurate data transmission. Strong technical knowledge of interoperability standards like HL7, DICOM, and FHIR is often required.
What are some common challenges faced in medical device integration roles?
Professionals in Medical Device Integration often encounter challenges such as managing compatibility across diverse devices and systems, troubleshooting intermittent connectivity issues, and complying with strict health data security regulations. The role frequently involves working with cross-functional teams, including IT, clinical staff, and device manufacturers, which requires clear communication and collaboration. Additionally, the rapid pace of technological advancements means team members must continually update their knowledge and adapt to new standards. Overcoming these challenges is not only rewarding but also critical to delivering seamless interoperability and improving clinical workflows.
What are the key skills and qualifications needed to thrive in medical device integration?
To thrive in Medical Device Integration, you need a solid understanding of medical devices, networking, HL7 interfaces, and healthcare IT systems, often supported by a degree in biomedical engineering, information technology, or a related field. Familiarity with integration engines (such as Mirth Connect or Cloverleaf), EHR platforms, and relevant certifications like CBET or CHTM is highly beneficial. Strong problem-solving, teamwork, and communication skills help in collaborating with clinicians, vendors, and IT staff. These competencies are essential for ensuring reliable and secure data flow between devices and healthcare systems, ultimately supporting patient care and operational efficiency.
What are popular job titles related to Medical Device Integration jobs in Wisconsin?
For Medical Device Integration jobs in Wisconsin, the most frequently searched job titles are:
What job categories do people searching Medical Device Integration jobs in Wisconsin look for?
The top searched job categories for Medical Device Integration jobs in Wisconsin are:
- Engineering Medical Device
- Product Manager Medical Device
- Temp Quality Engineer Medical Device
- Senior Complaint Handling Medical Device
- Per Diem Medical Device Sales
- Locum Medical Device Design
- Diabetes Territory Manager
- Cath Lab Sales
- Registered Nurse Medical Device Sales Representative
- Full Time Medical Device Reprocessing

Full-time
Re-posted yesterday
Job description
DuPont™ Spectrum™ Healthcare Solutions is seeking a New Product Development Engineer – Medical Films & Flexibles Packaging to drive advanced packaging design (films & conversion) & process development for critical healthcare and medical device applications. This technical role offers the opportunity to lead high-impact new product and process development programs from concept through commercialization within a world-class R&D and manufacturing environment. (Location – Pleasant Prairie, WI)
Role Overview
Lead end-to-end development of medical films and flexible packaging solutions, applying deep expertise to design, scale-up novel packaging technologies that meet stringent medical device requirements. Primary job scope includes hands-on new product and process development, and project leadership all the way from translating customer needs into innovative packaging designs and materials, through prototyping, pilot-scale process development, validation (IQ/OQ/PQ), and tech transfer to full-scale commercial launch. By applying scientific rigor and project management best practices, you will help expand and grow DuPont Spectrum Life Sciences medical films & packaging innovation portfolio, while ensuring regulatory compliance and quality reliable performance.
Key Responsibilities
- Flexibles Packaging New Product Design & Development: Ideate and develop new medical-grade films and flexible packaging form factors tailored for healthcare applications such as medical devices. Translate customer and application requirements into clear design specifications and structure–property-process hypotheses to optimize performance requirements such as barrier properties, mechanical strength, and compatibility with sterilization methods. Lead prototype development, process development, testing of films (multi-layer), laminates, and form factors (e.g. pouches, header bags, conversion films) that ensure sterile barrier integrity and durability for medical device packaging.
- Flexibles Packaging & Conversion Process Development: Develop and optimize polymer film extrusion (blown film) and packaging conversion processes (e.g. film casting, slitting, pouch forming, sealing). Scale up new products from prototyping concepts through pilot trials to manufacturing, ensuring processes are robust, efficient, and capable of high-quality output. Collaborate with manufacturing engineers on process scale-up and technology transfer to establish process parameters, standard operating, and procedures Troubleshoot complex process issues using root cause analysis, and implement corrective and preventive actions to continuously improve yield, reliability, and product quality.
- Project Management & Risk Mitigation: Lead and drive cross-functional new product development project teams through a structured stage-gate development process, from concept to commercial launch. Develop and manage project plans defining scope, timeline, resource needs, and critical milestones. Proactively identify and mitigate risks (technical, regulatory, or timeline) using risk management practices (e.g., DFMEA/PFMEA) and implement contingency plans to keep projects on track. Provide regular updates and data-driven reports on progress and utilize proper escalation to ensure project commitments on schedule, cost, and quality are met.
- Regulatory Compliance & Process Validation: Ensure all new packaging designs and processes meet medical device packaging standards and regulations (e.g., ISO 11607, FDA QSR, ISO 13485). Lead development of design verification and validation plans for packaging (including sterilization, shelf-life/aging, seal integrity, distribution simulation) and oversee execution of IQ/OQ/PQ process validations to demonstrate compliance and robust performance. Maintain meticulous technical documentation (specifications, protocols, reports) aligned with design control and quality system requirements throughout development.
- Customer Collaboration & Technical Leadership: Act as a customer-facing technical leader for healthcare packaging projects. Partner closely with medical device clients and internal teams (marketing, product management, quality, operations) to align development with customer needs and ensure successful product integration. Deliver clear and compelling technical presentations, progress updates, and design reviews to customers and stakeholders. Champion a customer-centric approach within R&D, ensuring excellent communication, service, and responsiveness to build confidence in DuPont’s packaging solutions.
- Continuous Improvement: Foster a culture of continuous improvement in packaging technology. Explore new materials, sustainable solutions, and advanced processing techniques (e.g., recyclable films, high-barrier coatings) to differentiate DuPont’s offerings. Apply statistical methods and data-driven problem-solving (Design of Experiments, DOE; process capability analysis; Minitab or similar tools) to characterize processes and optimize product performance. Document learnings, contribute to intellectual property (patents), and leverage insights to refine best practices and improve time-to-market for new products.
Qualifications
- Education & Experience: Bachelor’s degree in Materials Science, Polymer Science, Chemical Engineering, or related field with 10+ years of industry experience (or 5+ years experience with advanced degree (Masters or Ph.D.) in new product development, R&D, or process engineering roles. Demonstrated experience in polymer film extrusion and flexible packaging conversion processes is highly desired, especially for medical or pharmaceutical packaging applications.
- Medical Packaging & Regulatory Knowledge: Strong knowledge of medical device packaging requirements and standards (e.g., ISO 11607, ISO 13485, FDA regulations). Familiarity with sterilization processes (EtO, radiation, etc.) biocompatibility considerations. Experience with risk management and design control in regulated product development (FMEA, verification/validation, traceability) is a plus.
- Technical & Process Expertise: Hands-on skills in polymer processing and packaging engineering, including film extrusion, coating/lamination, thermoforming, sealing, and related testing methods. Proficiency in process development and validation (e.g., executing IQ/OQ/PQ), and in applying statistical analysis tools (DOE, Minitab or similar) for process optimization and problem solving. Ability to interpret engineering drawings and specifications for precise, high-quality components.
- Project Leadership & Collaboration: Proven ability to lead complex projects and coordinate cross-functional teams with minimum guidance. Strong project management skills capable of organizing and driving multiple projects to completion, balancing technical depth with timeline and budget constraints. Excellent communication and interpersonal skills, with a track record of effective collaboration across R&D, manufacturing, quality, regulatory, and commercial teams.
- Innovation & Problem-Solving: Creative thinker with a passion for innovation in materials and processes. Demonstrated success in solving challenging technical problems through analytical thinking and experimentation. Evidence of innovation outputs (such as patents, published research, or commercialized products) is valued.
- Drive & Adaptability: Self-motivated and results-oriented, able to thrive in a dynamic environment. Adaptable and resilient, with the ability to manage multiple priorities and adjust to evolving project needs. Committed to continuous learning, high-quality work, and professional growth.
- Travel Requirements: Willingness to travel up to 20% to support customer collaborations, off-site trials, or manufacturing activities as needed.
About Spectrum Plastics Group
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Alpharetta, GA, US
Year founded
1961