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Lead Engineer, R&D Innovation

hace 2 meses


San Francisco, Heredia, Costa Rica Boston Scientific A tiempo completo
About the Role

We are seeking a highly skilled and experienced Lead Engineer to join our R&D team at Boston Scientific. As a key member of our innovation team, you will be responsible for leading design changes originating from product or yield improvements, regulatory or supply chain needs.

Key Responsibilities
  • Develop and implement new technologies, products, materials, processes, or equipment with minimal supervision.
  • Independently or as a member of a team, develop plans, direct, and implement solutions.
  • Compile and analyze operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.
  • Develop technology, product designs, testing of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation.
  • Lead product improvement design activities.
  • Design, coordinate, analyze complex engineering tests and experiments.
  • Develop slide decks & reports and present updates to management & technical community.
  • Influence middle management on business solutions.
  • Interface with physicians, Marketing and/or field personnel to obtain feedback on concepts and performance of new devices.
  • Translate customer needs into product requirements and design specifications.
  • Partner with process development, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure success.
  • May train and/or provide work direction to technicians and entry-level engineers.
  • Establish and cultivate a wide range of business relationships to facilitate completion of assignments. May interact with vendors.
  • May lead projects within the function or department and/or represent a specialized field in larger project teams.
  • Use discretion, diplomacy and tact to resolve difficult situations. May escalate serious issues to manager.
  • Conduct root cause analysis of design related field complaints.
  • Support RA team with new markets registrations and regulatory submissions.
Requirements
  • Experience: > 5 years
  • English level: 80-89% or above
  • Licenciature: Mechanical, Electromechanical, Biomedical or related field
  • Master degree desirable
  • Problem solving
  • Technical and Clinical Knowledge
  • Networking
  • Design control methods such as Risk Analysis (dFMEA, pFMEA)
  • Design, Validation and Verification plans, protocol, and report generation.
  • Medical Devices Industry experience
  • PDP/TDP System
  • Preferred Project management
  • Please submit Resume in English