Research And Development Engineer
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-02-16
Listing for:
KKR Consulting
Full Time
position Listed on 2026-02-16
Job specializations:
-
Engineering
Biomedical Engineer, Quality Engineering, Medical Device Industry
Job Description & How to Apply Below
KKR Consulting partners with businesses to solve challenges, streamline processes, and achieve lasting success. We specialize in providing tailored consulting services across Aerospace, Medical Devices, Automotives, Pharmaceuticals, and Biotechnology industries, helping clients drive innovation, enhance operations, and achieve sustainable growth.
Job Title:R&D Engineer
Job Summary
The R&D Engineer will support the design, development, and verification of innovative medical devices in a highly regulated environment. This role focuses on hands-on engineering execution, design controls, and cross-functional collaboration to ensure products meet performance, safety, and regulatory requirements throughout the product development lifecycle.
Key Responsibilities- Support design and development of medical device components and systems from concept through commercialization
- Create and maintain engineering documentation in compliance with design control requirements
- Perform verification and validation (V&V) testing and support protocol/report development
- Participate in risk management activities (hazard analysis, FMEA)
- Support design reviews, technical assessments, and change control activities
- Collaborate with cross-functional teams including Quality, Regulatory, Manufacturing, and Clinical
- Assist with failure analysis, troubleshooting, and root cause investigations
- Support manufacturing transfer and product sustaining activities
- Bachelor’s degree in Engineering (Mechanical, Biomedical, Electrical, or related field)
- 5 years of experience in medical device R&D or regulated product development
- Working knowledge of design controls and product development lifecycle
- Experience with V&V testing and technical documentation
- Familiarity with FDA and ISO 13485 requirements
- Strong analytical, documentation, and communication skills
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