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R&D Specialist
R&D SpecialistKelly Science, Engineering, Technology & Telecom • Irvine, CA, US
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R&D Specialist

R&D Specialist

Kelly Science, Engineering, Technology & Telecom • Irvine, CA, US
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Kelly Engineeringis hiring an R&D Specialist for a long-term contract at one of our Global Medical Device clients. We are searching for a driven and detail-oriented R&D Specialist with medical device industry experienceto join an innovative team based in Irvine, California

This position is a specialist in supporting project teams in the development of electrophysiology catheters and / or related accessories. The project coordinator works directly with the team to coordinate activities related to new product development and the lifecycle.

Key Responsibilities :

  • Manufacturing line support and DHR audit experience
  • Being a self-starter is important in this role
  • Lead the execution, audit, and closure of work orders
  • Function as Project Coordinator for the Device History File of a project team
  • Manage the supply chain for new product development materials
  • Manage inventory of new product development materials
  • Kit materials for new product development builds while maintaining traceability
  • Maintain design control for new product development build activities
  • Supports project team / technical projects and initiatives that focus on cost improvement, business continuity, process excellence to enable product development activities
  • Support Compliance activities
  • Responsible for coordinating and tracking training for team associates
  • Monitor and report on project budget expenses
  • Support the project team in the creation and reconciliation of purchase order requisitions
  • Monitor and report on budget spend in anticipation of quarterly and fiscal year close
  • Coordinate logistics and payment for physician engagements and project studies
  • Coordinate requests for HCP & non-HCP engagement, travel, and research contracts
  • Supports projects / initiatives to enable product development activities

Required Qualifications :

  • Medical device experience is required
  • Manufacturing line support and DHR audit experience
  • In-depth knowledge of MS Office (i.e. Excel, Word, Outlook, and PowerPoint)
  • Knowledge of PLM systems (i.e. JDE, Windchill)
  • Ability to work with internal engineers & external vendors, detail-oriented to track progress
  • Excellent verbal and written communication skills
  • Exceptional aptitude in multitasking
  • In depth understanding of specialized area to support new product development and lifecycle management (Product structure, Bills of Material, routings, etc.)
  • Decision-making ability
  • Self-motivated and project-oriented, whether independently or with a team
  • Good sense of urgency
  • Strong technical skills are required
  • Knowledge and experience in product development processes a plus
  • Locate sources for engineering materials and services, obtain quotes and place orders for material and services
  • Support communication activities regarding R&D initiatives
  • Some program management duties as assigned
  • Must be able to provide and utilize your own laptop
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    Rd • Irvine, CA, US

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