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Medical Device Research And Development Jobs in Wisconsin

Smiths Machine

Product Development Engineer

Kenosha, WI · On-site

$90K - $110K/yr

Compiles and analyzes operational, test, and research data to establish performance standards for ... Proven track record in medical device design and development. * Knowledge of emerging trends and ...

Nipro Europe Group Companies

WI · On-site

$138.14 - $195.70/hr

Extensive medical device R&D engineering experience within a regulated industry environment: ISO 13485, MDR,/FDA design control, IEC 60601, ISO 14971, Verification & Validation documentation for ...

New

Socket.dev

Regulatory Quality Engineer

Kenosha, WI · On-site

$90 - $120/hr

Leads and/or participates in the development, implementation, compliance, and maintenance of ... Knowledge of the medical device manufacturing industry. * Knowledge of ISO 13485 Quality Management ...

New

DuPont

WI · On-site

$79.95 - $125.64/hr

... medical device applications within the LiveoTM platform. This role is both customer-facing and ... Through close collaboration with commercial, R&D, and manufacturing teams, you will drive ...

New

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Medical Device Research And Development information

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

What are some typical challenges faced by professionals in medical device research and development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

What are the key skills and qualifications needed to thrive in medical device research and development, and why are they important?

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

What is the difference between Medical Device Research And Development vs Medical Device Quality Assurance?

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

What are popular job titles related to Medical Device Research And Development jobs in Wisconsin?

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

What job categories do people searching Medical Device Research And Development jobs in Wisconsin look for?

The top searched job categories for Medical Device Research And Development jobs in Wisconsin are:

Medical Device Research And Development jobs near you
Infographic showing various Medical Device Research And Development job openings in Wisconsin as of August 2026, with employment types broken down into 77% Full Time, 17% Part Time, and 6% Contract. Highlights an 100% In-person job distribution.

Director, Medical Business Development - Minneapolis, MN

Comar Engineering Services

Woodville, WI • On-site

$200K/yr

Full-time

Re-posted 18 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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