Sr R&d Scientist

Johnson & Johnson Johnson & Johnson · Pharma · Groningen, Netherlands

This role is for a Sr. R&D Scientist in the Vision team at Johnson & Johnson's MedTech division in Groningen, Netherlands. The scientist will participate in the development of new concepts for unique medical devices, specifically intraocular lenses and optical metrology. Responsibilities include developing test methods, validation systems, supporting design documentation, and conducting independent research with European institutes. The role requires a BS/MS/PhD in Optics, Physics, or Vision Science, proficiency in optical design tools, and demonstrated research experience.

What you'd actually do

  1. Participate in the development of new concepts for unique medical devices from ideation to market phase.
  2. Support and participate in design and development of new intraocular lenses and new optical metrology for testing intraocular lenses.
  3. Develop test methods and validation systems to characterize new and existing intraocular lenses.
  4. Support requirements development, documentation of design, writing and execution of protocols and reports.
  5. Stay current with the status of competitive products, with cutting-edge medical device industry and with technological trends to ensure innovative product design. Investigate and evaluate existing technologies.
  6. You will contribute to multi-disciplinary research teams and will be responsible for conducting independent research tasks with European research institutes.
  7. Work closely within a cross-functional team, with senior research staff, and also with research institutes and R&D groups in USA.

Skills

Required

  • Communication
  • Innovation
  • Problem Solving
  • Research and Development
  • BS/MS/PhD in Optics, Physics or Vision Science
  • Proficient in optical design principles, using Zemax, OSLO or other design tools to design and simulate optical systems
  • Demonstrated research experience and interest in technology development

Nice to have

  • Clinical Data Management
  • Clinical Evaluations
  • Coaching
  • Critical Thinking
  • Data Savvy
  • Drug Discovery Development
  • Ethical and Participant Safety Considerations
  • Good Clinical Practice (GCP)
  • Industry Analysis
  • Medicines and Device Development and Regulation
  • Regulatory Affairs Management
  • Relationship Building
  • Research Documents
  • Safety-Oriented
  • Scientific Research
  • Standard Scientific Processes and Procedures
  • Technologically Savvy
  • 3 or more years of relevant experience