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Principal R&D Engineer

Job in Sunnyvale, Santa Clara County, California, 94087, USA
Listing for: QUICK USA
Full Time position
Listed on 2026-06-18
Job specializations:
  • Engineering
    Biomedical Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

勤務地 Sunnyvale, California

業界 Manufacturing

職種 Engineering

給与 90K-150K

雇用形態 / 勤務形態 Full Time Permanent, On-site

Position

Principal R&D Engineer

Summary

Responsible for product development activities that encompass the design, testing, fabrication and validation of systems and devices as well as ancillary systems that may be necessary to meet company goals and objectives.

Essential Duties
  • Applies intensive and diversified knowledge of engineering principles and practices to the research, development, design and evaluation of technical suitability of materials, components, assemblies, processes and/or equipment. Clearly communicates designs and all requisite requirements to support personnel both verbally and in writing.
  • Works to improve and expand company's capabilities to provide R&D services.
  • Contributes to, develops and/or performs marketing and engineering specifications, feasibility plans/studies/reports, cost estimation/analysis, design reviews, risk and hazard analyses, FMEAs for Design/Process/Use, product verification and validation testing.
  • Builds and implements a detailed research/development work plan to fulfill company's project objectives.
  • Directs support personnel and coordinates their project activities.
  • Develops prototypes and processes based on company's available equipment, processes and/or specifies, procures suitable equipment for development reviews or coordinates supplier activities to support development.
  • Analyzes, recommends and implements process improvements that reduce lead-time, eliminate non-valued added work, improve yields, and improve process capabilities.
  • Manually builds prototypes in accordance with engineering instructions, drawings and specifications.
  • Writes and submits intellectual property disclosures (patents). Attends animal studies as needed.
  • Ensures appropriate communication processes are established within and across functional groups. Communicates information related to quality management system effectiveness. Works in accordance with quality system procedures.
  • Collaborates with medical professionals during all stages of development of prototypes/products, including market/product specification development, pre-clinical and clinical testing of prototypes/products.
  • Other duties as assigned.
Working Hours, Working Style

8:00-17:00

Working Location

Sunnyvale, CA

Salary, Benefit
  • 90K-150K
    * DOE
  • 401K 4%
  • Bonus
  • Insurance
Holidays

Saturdays, Sundays, holidays

Qualifications
  • BS degree in Biomedical, Mechanical, or Biomedical Science or related degree. Under certain circumstances, and at Management’s discretion, specific training and/or experience may fulfill the requirements of this position.
  • 5+ years medical design experience in medical device/clinical environment.
  • 2-3 years of team lead or supervisor experience
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