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Manager R&D Engineer Medical Device Jobs in California

Minimum of 2 years of engineering experience in product development or manufacturing within a regulated medical device industry. [1] * Technical Skills: Strong working knowledge of SolidWorks for 3D ...

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Project Manager - R.D. Olson Construction | SoCal Southern California | Commercial GC | Hospitality ... engineering wins and track profitability ✔ Mentor PEs and APMs -- grow the next generation ✔ ...

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Senior Mechanical Engineer - Medical Device San Diego, CA (Onsite) 130,000-180,000 DOE Join a growing medical-device team developing and improving a precision electromechanical product. This is an ...

Manage and logically organize data to identify and describe problems and assess the suitability and ... values of R.E.S.P.E.C.T. and the Mizuho OSI Way. • Create innovative solutions designed and ...

Project Manager

Irvine, CA · On-site

$96K - $140K/yr

Project Manager - R.D. Olson Construction | SoCal Southern California | Commercial GC | Hospitality ... engineering wins and track profitability • Mentor PEs and APMs - grow the next generation • ...

Project Manager - R.D. Olson Construction | SoCal Southern California | Commercial GC | Hospitality ... engineering wins and track profitability ✔ Mentor PEs and APMs -- grow the next generation ✔ ...

... Systems Engineer you will be part of a small, agile team; responsible for medical device ... Develop, manage and maintain design history files and related deliverables. * Develop, maintain and ...

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Manager R D Engineer Medical Device information

What are the most commonly searched types of R&D Engineer Medical Device jobs in California?

The most popular types of R&D Engineer Medical Device jobs in California are:

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Cities in California with the most Manager R&D Engineer Medical Device job openings:

Full-time

Posted 3 days ago

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Job description

Essential Job Functions

  • Design & Prototyping: Build preliminary sketches, 3D models, detailed design concepts, and engineering prototypes. [1]
  • Testing & Validation: Plan and run benchtop tests, verification and validation (V&V), and pre-clinical studies, writing clear protocols and reports. [1]
  • Tooling: Make tools, jigs, and fixtures to help with testing, prototyping, and manufacturing. [1]
  • Documentation: Write product drawings, risk analysis, specifications, and keep the Design History File (DHF) updated for regulatory compliance. [1]
  • Collaboration: Help with product transfer, scale-up activities, and share new ideas to grow the company's patent and intellectual property base. [1]
  • Lab Support: Keep the R&D lab clean and organized for smooth prototype development. [1]

Job Requirements

  • Education: Bachelor's degree or higher in Biomedical, Mechanical, or Materials Engineering. [1]
  • Experience: Minimum of 2 years of engineering experience in product development or manufacturing within a regulated medical device industry. [1]
  • Technical Skills: Strong working knowledge of SolidWorks for 3D modeling and engineering drawings. [1]
  • Core Skills: Good problem-solving abilities, strong technical writing skills, and familiarity with FDA submissions, ISO standards, and Quality System Regulations (QSR)