R&D Engineer

Karwell Technologies

San Jose, CA

JOB DETAILS
SKILLS
Aerospace and Defense, Analysis Skills, AutoCAD, Biology, Biomedical Engineering, Biotech and Pharmaceutical, CAD (Computer-Aided Design) Software, CATIA CAD, Code of Federal Regulations, Communication Skills, Continuous Improvement, Corrective Action, Cross-Functional, Data Analysis, Design Failure Mode and Effects Analysis (DFMEA), Design Verification, Detail Oriented, Documentation, Electrical Engineering, Engineering Drawing, Experiment Design, FDA (Food and Drug Administration), Failure Mode and Effects Analysis (FMEA), Feasibility Analysis, Geometric Dimensioning and Tolerancing, ISO (International Organization for Standardization), ISO 9001, Identify Issues, Industrial Engineering, Industry Standards, Maintain Compliance, Manufacturing, Manufacturing Engineering, Manufacturing/Industrial Processes, Mechanical Engineering, Medical Equipment, Minitab, Operational Support, PTC Creo, Presentation/Verbal Skills, Problem Solving Skills, Process Failure Mode and Effects Analysis (PFMEA), Process Improvement, Process Validation, Product Design, Product Development, Product Lifecycle, Product Programs, Product Support, Product Testing, Product/Service Launch, Prototyping, Quality System Requirements (QSR), Regulations, Regulatory Compliance, Regulatory Requirements, Reporting Skills, Research & Development (R&D), Risk Analysis, Risk Management, Root Cause Analysis, Siemens PLM Software NX (fka UGS NX), SolidWorks, Statistics, Supply Chain Operations, Technical Presentation, Technical Writing, Technical/Engineering Design, Test Data, Test Plan/Schedule, Testing, Tolerance Analysis, United States Department of Energy (DOE), V&V Testing, Validation Testing, Writing Skills
LOCATION
San Jose, CA
POSTED
9 days ago
Job Description:
We are seeking an innovative and detail-oriented R&D Engineer to support the research, design, development, and validation of new products and technologies. The ideal candidate will collaborate with cross-functional teams to transform concepts into commercially viable products while ensuring compliance with quality, regulatory, and customer requirements. This role involves product design, prototyping, testing, risk analysis, design verification and validation, and continuous product improvement throughout the development lifecycle.
Responsibilities:
  • Design, develop, and improve new products, components, and manufacturing processes.
  • Support all phases of product development, from concept through commercialization.
  • Create engineering drawings, specifications, and technical documentation.
  • Develop prototypes and conduct feasibility studies to evaluate product performance.
  • Plan and execute design verification and validation (V&V) testing.
  • Perform root cause analysis and implement corrective actions for product and process issues.
  • Conduct Design Failure Mode and Effects Analysis (DFMEA), Process FMEA (PFMEA), and risk assessments.
  • Collaborate with Manufacturing, Quality, Regulatory, Supply Chain, and Operations teams to support design transfer and production readiness.
  • Support process validation activities, including IQ/OQ/PQ, as required.
  • Analyze test data and prepare engineering reports and technical presentations.
  • Ensure compliance with applicable industry standards, regulatory requirements, and company quality systems.
  • Drive continuous improvement initiatives to enhance product quality, reliability, and manufacturability.
  • Participate in design reviews, technical risk assessments, and engineering change activities.

Requirements:

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Manufacturing Engineering, Industrial Engineering, or a related engineering discipline.
  • 3 8+ years of experience in Research & Development, Product Development, or Design Engineering.
  • Experience with product design, prototype development, testing, and engineering documentation.
  • Proficiency in CAD software such as SolidWorks, Creo, CATIA, AutoCAD, or Siemens NX.
  • Strong understanding of engineering principles, materials, and manufacturing processes.
  • Experience with Design Verification & Validation (V&V).
  • Knowledge of Design Controls, Risk Management, and Design Reviews.
  • Strong analytical, problem-solving, and troubleshooting skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in a cross-functional team environment.

Preferred Qualifications:

  • Experience in Medical Devices, Biotechnology, Life Sciences, Aerospace, Automotive, Consumer Products, or Advanced Manufacturing.
  • Knowledge of ISO 13485, FDA 21 CFR Part 820/QMSR, ISO 14971, or ISO 9001 (depending on industry).
  • Experience with statistical analysis tools such as Minitab or JMP.
  • Familiarity with DOE (Design of Experiments), GD&T, tolerance analysis, and DFM/DFA principles.
  • Experience supporting New Product Introduction (NPI) and design transfer activities.

About the Company

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Karwell Technologies