Medical Device R&d Engineer

ZEISS Group

Reno, NV, USA
Not specified (assumed to be in-person based on the nature of the role)
Product and process development
Design verification and validation testing
Cad solid models and drawings
The ZEISS Group is seeking a Medical Device R&D Engineer in Reno, NV, to lead product and process development projects within the R&D/Operations group. The ideal candidate will have extensive experience in medical device engineering, particularly in regulated environments, and will be responsible for overseeing complex projects and mentoring junior team members

Job Summary

  • Leads and drives the execution of complex product and process development programs, ensuring alignment with strategic objectives and Company milestones.
  • Provides expert technical guidance and direction to team members, assembly personnel, and external consultants engaged in R&D/OPS initiatives.
  • Collaborate cross-functionally to identify project priorities, coordinate efforts across departments and resolve complex technical or process challenges, providing strategic recommendations that drive innovation, efficiency and the successful advancement of ophthalmology product development programs.

Matching Summary

Match Score: 85

The ZEISS Group is seeking a Medical Device R&D Engineer in Reno, NV, to lead product and process development projects within the R&D/Operations group. The ideal candidate will have extensive experience in medical device engineering, particularly in regulated environments, and will be responsible for overseeing complex projects and mentoring junior team members.

Skills & Requirements

Must-have

  • Product and process development
  • Design verification and validation testing
  • CAD solid models and drawings
  • Medical device regulations
  • Cross-functional collaboration

Nice-to-have

  • Ophthalmology product development
  • Supplier relationship management
  • Mentoring junior engineers
  • Innovation in production development

Key Requirements

  • Bachelors in engineering or related field
  • Minimum five years’ engineering experience
  • Experience in regulated medical device environment
  • Familiarity with 510(k) and MDR
  • SolidWorks/Cad experience
  • FDA 21 CFR Part 820, ISO 13485 knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter