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Research & Development – Medical Device Product Development Professional - P3

RDMDPD2.GEN.P3

P3P3 — Mid-Level Professionalmedium0.70draftglobalv1

An experienced medical device professional who serves as a key contributor and technical lead within product development projects.

Summary

An experienced medical device professional who serves as a key contributor and technical lead within product development projects.

Level — P3 — Mid-Level Professional

Fully competent professional; works independently on standard projects

Scope
Features or a sub-system end-to-end
Autonomy
Works independently on standard work; reviewed on the non-standard
Complexity
Diverse problems; adapts existing approaches
Impact
Project / team outcomes
Decision rights
Owns implementation decisions for own scope
Leadership
Mentors juniors informally
Typical experience
3–5 yrs

Core outputs

No core outputs recorded yet.

Adjacent roles

Nearest roles by structural coordinates (level + taxonomy). Distance 0 → 1; each carries its 3-state match band. How coordinates work →

Components

Responsibilities16

  • Lead the design and development of medical device componentscommonlevel
  • Plan and manage project tasks and timelinescommonlevel
  • Drive meaningful innovation by researching emerging technologiescommonlevel
  • Ensure project deliverables meet quality and regulatory standardscommonlevel
  • Mentor junior engineers and provide technical guidancecommonlevel
  • Coordinate with cross-functional teams for project successcommonlevel
  • Develop and implement testing protocolscommonlevel
  • Prepare and present technical reports to stakeholderscommonlevel
  • Create and refine device designs using engineering principles and CAD software.commonlevel
  • Plan and conduct bench tests, simulations, and experiments to evaluate device performance.commonlevel
  • Ensure compliance with quality standards and regulatory guidelines.commonlevel
  • Collaborate with cross-functional teams to optimize product designs.commonlevel
  • Document design processes and test results for regulatory submissions.commonlevel
  • Identify and resolve engineering issues during the development process.commonlevel
  • Contribute to risk management activities and design reviews.commonlevel
  • Support manufacturing teams in transitioning products from development to production.commonlevel

Tasks6

  • Lead design and development projectscommonlevel
  • Manage project timelines and deliverablescommonlevel
  • Research and integrate emerging technologiescommonlevel
  • Design and refine medical devicescommonlevel
  • Conduct performance testscommonlevel
  • Ensure regulatory compliancecommonlevel

Skills14

  • Advanced CAD skillscommonlevel
  • Project managementcommonlevel
  • Technical leadershipcommonlevel
  • Regulatory strategycommonlevel
  • Innovation techniquescommonlevel
  • Stakeholder communicationcommonlevel
  • Risk assessmentcommonlevel
  • Problem-solvingcommonlevel
  • CAD designcommonlevel
  • Engineering analysiscommonlevel
  • Regulatory compliancecommonlevel
  • Communicationcommonlevel
  • Teamworkcommonlevel
  • Documentationcommonlevel

Knowledge15

  • Advanced engineering principlescommonlevel
  • Project management methodologiescommonlevel
  • Regulatory compliancecommonlevel
  • Innovation in medical devicescommonlevel
  • Quality management systemscommonlevel
  • Strategic planningcommonlevel
  • Emerging technologiescommonlevel
  • Cross-functional collaborationcommonlevel
  • Medical device regulationscommonlevel
  • Engineering principlescommonlevel
  • Product lifecycle managementcommonlevel
  • Quality assurancecommonlevel
  • Risk managementcommonlevel
  • Design for manufacturabilitycommonlevel
  • Testing and validationcommonlevel

competency15

  • Independent leadershipcommonlevel
  • Analytical thinkingcommonlevel
  • Excellent communication skillscommonlevel
  • Project managementcommonlevel
  • Innovationcommonlevel
  • Regulatory knowledgecommonlevel
  • Team leadershipcommonlevel
  • Strategic planningcommonlevel
  • Strong analytical and problem-solving skillscommonlevel
  • Good communication skillscommonlevel
  • Proficiency in CAD softwarecommonlevel
  • Knowledge of regulatory standardscommonlevel
  • Team collaborationcommonlevel
  • Attention to detailcommonlevel
  • Adaptabilitycommonlevel

qualification7

  • Bachelor’s degree in Engineeringcommonlevel
  • 5-8+ years of experience in medical device R&Dcommonlevel
  • Advanced degree (M.S. or Ph.D.) in a relevant fieldcommonlevel
  • Familiarity with the full product development lifecyclecommonlevel
  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering or a related fieldcommonlevel
  • 3–5 years of hands-on experience in medical device developmentcommonlevel
  • A Master’s degree in a relevant engineering discipline (preferred)commonlevel

Title aliases

AliasTypeConfidenceApproved
Research & Development – Medical Device Product Development Professional - P3commonmedium0.60
Senior R&D Engineercommonmedium0.50
Research & Development – Medical Device Product Development Product Development Engineer (Mid-Level)commonmedium0.60
Mid-Level Professionalcommonmedium0.50

Classification mappings

O*NET / SOC

  • code=19-0000title=Life, Physical, & Social Science Occupationssource=inferred_from_superfunctionreviewStatus=needs_review