R&d Specialist 3

Johnson & Johnson

Irvine, California, United States of America
Base: $92,000.00 - $148,350.00; bonus/equity: not ...
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R&d specialist 3
Electrophysiology business support
New product development
** Johnson & Johnson is seeking an R&D Specialist 3 for their Electrophysiology team in Irvine, California. The role involves supporting project teams in the development of electrophysiology catheters and related accessories, with responsibilities ranging from sourcing engineering materials to managing project documentation. **

Job Summary

  • This role supports project teams in the development of electrophysiology catheters and/or related accessories at Biosense Webster, coordinating activities related to new product development and lifecycle.
  • Duties include sourcing engineering materials, managing supply chains, controlling inventory, maintaining design control, coordinating HCP contracts, team training, travel arrangements, and budget tracking.
  • Johnson & Johnson is committed to fostering an inclusive work environment where diversity and individual merit are recognized and respected.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking an R&D Specialist 3 for their Electrophysiology team in Irvine, California. The role involves supporting project teams in the development of electrophysiology catheters and related accessories, with responsibilities ranging from sourcing engineering materials to managing project documentation. **

Salary

Base: $92,000.00 - $148,350.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours for an immediate family member, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours per calendar year, Military Spouse Time-Off – 80 hours per calendar year

Skills & Requirements

Must-have

  • R&D Specialist 3
  • Electrophysiology business support
  • New product development
  • Supply chain management
  • Design control
  • Windchill PLM system experience

Nice-to-have

  • Action-Oriented
  • Agility Jumps
  • Business Alignment
  • Business Behavior
  • Collaborating
  • Continuous Improvement
  • Execution Focus
  • Operations Management
  • Problem Solving
  • Process Improvements
  • Project Management Methodology (PMM)
  • Project Management Office (PMO)
  • Project Reporting
  • Project Schedule
  • Quality Control (QC)
  • Research and Development
  • Stakeholder Engagement
  • AutoCAD experience

Key Requirements

  • 4 to 6 years of experience
  • University/Bachelors Degree or Equivalent
  • In depth understanding of specialized area
  • In depth understanding of new product development cost drivers
  • R&D finance and/or contracting process
  • Ability to work with various engineers & vendors
  • Must possess excellent communication skills
  • Exceptional aptitude in multitasking
  • Ability to utilize office computer programs proficiently
  • Must be detail oriented and highly organized
  • Communicate with other functions within the organization daily
  • Manages inventory for clinical investigational materials
  • Maintains traceability for clinical builds and approval for distribution
  • Assist in the development of test reports, generating ECOs and other engineering documentation
  • Responsible for timely presenting of business related issues or opportunities to next management level
  • Responsible for ensuring personal and Company compliance with all Federal, State, local and company regulations, policies and procedures

Work Rights

Not specified

Tailored Resume

Cover Letter