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Medical Device Product Development Engineer Jobs in Wisconsin

Promega

Product Design Engineer, IoT

Madison, WI · On-site

$130K - $156K/yr

As market demands evolve, this role may contribute to the development of medical devices, requiring ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Promega

Product Design Engineer, IoT

Madison, WI · On-site

$130K - $156K/yr

As market demands evolve, this role may contribute to the development of medical devices, requiring ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Promega

Product Design Engineer, IoT

Madison, WI · On-site

$130K - $156K/yr

As market demands evolve, this role may contribute to the development of medical devices, requiring ... Contribute to risk management and traceability documentation aligned with medical device lifecycle ...

Kellton Tech

Medical Device Quality Engineer

Madison, WI · On-site

$40 - $45/hr

Manage data collection and reporting for product recalls * Perform Quality System trending to ... Process Development. Must thrive in a fast-paced environment with strict timelines. Primarily ...

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All JobsMedical Device Product Development Engineer JobsMedical Device Product Development Engineer Jobs in Wisconsin

Medical Device Product Development Engineer information

See Wisconsin salary details

$39.9K

$88.7K

$133.7K

How much do medical device product development engineer jobs pay per year?

As of Aug 15, 2026, the average yearly pay for medical device product development engineer in Wisconsin is $88,706.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,700.00 and $100,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a medical device product development engineer?

To thrive as a Medical Device Product Development Engineer, you need a strong background in biomedical, mechanical, or electrical engineering, along with knowledge of FDA regulations and product development processes. Familiarity with CAD software, prototyping tools, risk management systems, and regulatory standards such as ISO 13485 is typically required. Creativity, problem-solving, and effective teamwork are essential soft skills that drive innovation and ensure project success. These skills and qualifications are crucial for developing safe, effective medical devices that meet strict regulatory requirements and address real-world healthcare needs.

What are some common challenges medical device product development engineers face when working on new product designs?

Medical Device Product Development Engineers often navigate strict regulatory requirements and rigorous testing protocols to ensure product safety and compliance. Balancing innovative design with manufacturability and cost constraints can be challenging, as can coordinating input from cross-functional teams such as clinical, regulatory, and manufacturing. Additionally, managing project timelines while accommodating iterative design changes based on feedback or testing results requires strong organizational and communication skills.

What does a medical device product development engineer do?

A Medical Device Product Development Engineer is responsible for designing, developing, and testing medical devices to ensure they are safe, effective, and compliant with regulatory standards. They work closely with cross-functional teams, including quality assurance, regulatory affairs, and manufacturing, to take products from concept through to production. Their tasks often include prototyping, risk assessment, documentation, and troubleshooting any issues that arise during the development process. Additionally, they must stay updated on industry standards and regulations to ensure that products meet all necessary requirements for market approval.

What is the difference between Medical Device Product Development Engineer vs Quality Assurance Engineer?

AspectMedical Device Product Development EngineerQuality Assurance Engineer
CredentialsEngineering degree, certifications like PMP or Six Sigma often preferredEngineering or science degree, certifications like CQE or ISO auditor training
Work EnvironmentDesign labs, R&D departments, cross-functional teamsManufacturing facilities, quality control labs, compliance departments
Industry UsageInvolved in designing and developing new medical devicesEnsures products meet quality standards and regulatory requirements

While both roles are essential in the medical device industry, the Medical Device Product Development Engineer focuses on creating and improving devices, whereas the Quality Assurance Engineer ensures these devices meet safety and quality standards. Understanding these differences helps in choosing the right career path or job search focus.

What are popular job titles related to Medical Device Product Development Engineer jobs in Wisconsin?

For Medical Device Product Development Engineer jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Medical Device Product Development Engineer jobs in Wisconsin look for?

The top searched job categories for Medical Device Product Development Engineer jobs in Wisconsin are:

Medical Device Product Development Engineer jobs near you
Infographic showing various Medical Device Product Development Engineer job openings in Wisconsin as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $88,706 per year, or $42.6 per hour.

Director, Medical Business Development - Minneapolis, MN

Comar Engineering Services

Woodville, WI

$200K/yr

Full-time

Re-posted 14 days ago

Job description

Job Summary

The Business Development Director is a strategic hunter responsible for securing new business with targeted medical device OEMs. The primary focus is proactive prospecting, penetrating new strategic accounts, and navigating complex customer organizations to identify and engage key decision-makers across R&D, engineering, supply chain, and executive leadership.

Key ResponsibilitiesStrategic Prospecting & New Account Acquisition
  • Identify and target new strategic medical OEMs aligned with PCI’s injection molding and contract manufacturing capabilities
  • Conduct structured prospecting using existing network, market intelligence, secondary industry networks, conferences, and CRM data to build a qualified target account list
  • Leverage knowledge gained from previously working with Medical OEM’s and network to help open doors for future project discussion
  • Map customer organizations and navigate to key decision-makers in R&D, product development, sourcing, and executive leadership
  • Initiate and lead discovery discussions to uncover unmet manufacturing needs and position PCI’s turnkey solutions and execute a minimum of 6 face to face meetings per month
  • Execute persistent, detail-oriented follow-up to advance early-stage opportunities into RFQs and awarded programs
Pipeline Development & Opportunity Conversion
  • Build and maintain a high-value, forward-looking pipeline focused on new customers and new programs (Goal of $40M in vetted pipeline opportunities per year)
  • Qualify opportunities based on technical fit, open capacity, strategic value, timeline, and margin potential (New opportunities to generate +$200K in annual revenues at ramp – open to discussions for smaller niche opportunities)
  • Drive opportunities from initial contact through DFM, quotation, negotiation, and award
  • Maintain accurate CRM data including stage progression, probability, next actions, and close timelines
  • Demonstrate a strong sense of urgency in progressing opportunities and meeting customer response timelines
Solution-Based Selling for Regulated Manufacturing
  • Position PCI’s full product lifecycle capabilities including DFM, tooling/automation strategy,  and validation (IQ/OQ/PQ) to production
  • Translate customer product concepts into manufacturable injection molding solutions in collaboration with engineering and operations
  • Deliver pipeline opportunities into actual program quotations - Lead meetings with the technical and commercial teams to shape opportunities prior to or shortly after RFQ release
  • Support development of cost models and pricing strategies that meet target margins and program risk profiles
Market Intelligence & Strategic Targeting
  • Monitor medical device as well as other medical vertical trends to identify emerging opportunities
  • Develop target account lists aligned with PCI’s technology roadmap and capacity strategy
  • Provide competitive insights and customer feedback to support strategic planning
Qualifications
  • Bachelor’s degree in business, Engineering, Life Sciences, or related field preferred
  • 10+ years of business development experience in medical injection molding or contract manufacturing
  • Demonstrated success in a hunter role securing new medical OEM customers
  • Proven ability to prospect, penetrate complex organizations, and reach technical and executive decision-makers
  • Experience selling into regulated environments (FDA, ISO 13485) with knowledge of DFM, tooling, and validation processes
  • Travel up to 50%

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