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Medical Device Research And Development Jobs in Kansas

Proven

Senior Systems Engineer

Olathe, KS · On-site

$98K - $135K/yr

The Systems Engineer leads a development team to document, analyze, mitigate risks, create, test, and help with the manufacturing of complex electromechanical and embedded medical device systems ...

Proven

Senior Systems Engineer

Olathe, KS · On-site

$98K - $135K/yr

The Systems Engineer leads a development team to document, analyze, mitigate risks, create, test, and help with the manufacturing of complex electromechanical and embedded medical device systems ...

Innovo Research

Clinical Research Coordinator

Hutchinson, KS · On-site

$21 - $28/hr

Understanding of medical terminology * Working knowledge of clinical trials * Knowledge and ability ... device. * In-depth knowledge of departmental, protocol, and study-specific operating procedures ...

ProPharma Group

... R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs. The Medical ...

Vantage MedTech

Customer Excellence Manager

Olathe, KS · On-site

VMT's capabilities cover the complete spectrum of the medical device manufacturing product life cycle, from conceptual design, engineering, prototype development, and regulatory support through ...

Rishabh RPO

Senior Systems Engineer

Olathe, KS · On-site

$101K - $138K/yr

The Systems Engineer leads a development team to document, analyze, mitigate risks, create, test, and help with the manufacturing of complex electromechanical and embedded medical device systems ...

IQVIA

Virtual Customer Engagement Specialist

Kansas City, KS · On-site

$23 - $26.44/hr

Our teams help biopharma, medical device and diagnostic companies get their therapies to the people ... We create intelligent connections to accelerate the development and commercialization of innovative ...

Vantage MedTech

Senior Systems Engineer

Olathe, KS · On-site

$98K - $135K/yr

The Systems Engineer leads a development team to document, analyze, mitigate risks, create, test, and help with the manufacturing of complex electromechanical and embedded medical device systems ...

Varsity Tutors

Biomedical Engineering Tutor

Wichita, KS · Remote

$18 - $40/hr

... medical device design principles while preparing students for biomedical engineering coursework, research, and industry careers. * Conceptual Teaching & Problem-Solving: Skilled at breaking down ...

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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 Kansas?

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

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

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

What cities in Kansas are hiring for Medical Device Research And Development jobs?

Cities in Kansas with the most Medical Device Research And Development job openings:

Medical Device Research And Development jobs near you
Infographic showing various Medical Device Research And Development job openings in Kansas as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, 1% Temporary, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Senior Systems Engineer

Proven

Olathe, KS • On-site

$98K - $135K/yr

Full-time

Posted 25 days ago

Job description

Proven is hiring a Senior Systems Engineer on behalf of our client, an industry innovator in comprehensive design and manufacturing services for cutting-edge medical technologies. Supporting the advancement of healthcare solutions from initial concept to full product realization, our client develops and manufactures critical devices used in treating heart failure, cancer, stroke, gene therapy, and other complex medical conditions.


The Systems Engineer leads a development team to document, analyze, mitigate risks, create, test, and help with the manufacturing of complex electromechanical and embedded medical device systems, including both software and hardware aspects with Embedded, Real-time, PC, Linux, and Windows applications. The Systems Engineer III collaborates with cross functional engineering team in all stages of new product development from requirements management and system architecture to product commercialization and Manufacturing. The Systems Engineer III often consults with clients to determine system specifications and write requirements. Provides technical expertise, guidance, and mentorship to Systems Engineers. Collaborates with PMs to develop proposals.
Key Responsibilities

  • Lead systems engineering activities, including requirements development, system architecture, and product design for medical device projects.
  • Collaborate with cross-functional teams, including software, electrical, mechanical, manufacturing, process, and test engineers throughout the product lifecycle.
  • Analyze customer and product requirements to define system-level specifications and ensure alignment with business and technical objectives.
  • Develop and execute verification and validation strategies, including test plans, procedures, protocols, and reports.
  • Maintain requirements traceability and ensure compliance with design control, quality, and regulatory requirements.
  • Troubleshoot and resolve complex system, hardware, software, and product design issues to support successful project execution.
  • Participate in risk management activities, design reviews, and phase gate reviews to ensure product safety, performance, and compliance.
  • Support product development from concept through commercialization, including manufacturing transfer and production support activities.
  • Mentor and provide technical guidance to junior engineers while driving engineering best practices and process improvements.
  • Partner with project managers, clients, clinicians, and other stakeholders to deliver innovative solutions on schedule and within budget


Education and Experience

  • Bachelor's degree in mechanical, electrical, or related engineering field
  • 8-10 years of professional experience in electromechanical and embedded systems product development
  • Experience with medical device development under quality systems
  • Experience with Source Code Management, Requirements Management, and Defect Tracking systems
  • Experience providing written reports, test protocols, and engineering documentation for the testing of medical devices
  • Experience with "white box" testing and automated testing
  • Experience with FDA class II or III medical device regulatory requirements, or experience in similar regulated product development environment
  • Advanced knowledge of ISO 13485/14971, 93/42/EEC, 90/385/EEC, EN45502, EN60601-1, EN61000.
  • Demonstrated project leadership skills

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