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Research and Development Engineering is responsible for development and lifecycle management of products through medical device design control processes and good engineering and documentation practices. The Infusion Preparation and Delivery (IPD) platform seeks a hardworking and passionate leader to develop and drive technical strategies. Demonstrates working knowledge of Engineering principles and its application in solving standard technical problems. Demonstrates working knowledge of product design, development, and design control process. Develops technical plans for design inputs and outputs, conducts analytical and empirical feasibility studies, develops test methods to verify and validate subsystems and systems to transfer designs alongside Manufacturing. Demonstrates knowledge to provide design documentation to support global Regulatory filing strategies. Collaborates within a cross-functional team to plan, develop, modify, implement, and support IPD products through the application of rigorous engineering practices. Works with moderate guidance to achieve project objectives. R&D engineers are responsible for leading and supporting projects as part of a cross-functional global team.
Job Responsibility:
Lead R&D deliverables throughout the medical device design control process for intravenous infusion sets and connection devices
Collaborate within a cross-functional team to plan, develop, modify, implement, and support IPD products through the application of rigorous engineering practices
Engineer robust products through strong understanding and application of engineering fundamentals and DFSS principles
Develop technical plans and guide the team to develop design inputs, conduct analytical and empirical feasibility studies, refine product configurations and designs, verify, and validate subsystems and systems, concurrently transfer designs alongside Manufacturing and Operations, and provide design documentation to support global Regulatory filing strategies
Projects will involve requirements definition, developing test methods, writing test protocols, reports, executing verification testing, solving test or design issues and other types of mechanical engineering activities
Requirements:
5yr experience regulated devices and Engineering degree or 3yr experience regulated devices and Engineering degree with Masters
BS – Mechanical Engineering, Materials Engineering or Biomedical Engineering
Work experience 5 years or 3 years plus an advanced degree
Critical thinking – able to work with moderate guidance in own area of knowledge
SolidWorks or equivalent CAD tool
Ability to manage multiple projects of varying scopes in parallel
Ability to work leading or as part of a cross-functional team with members from marketing, sales, clinical, regulatory, medical affairs, quality, manufacturing, etc.
Experience with medical device design control processes and creating and maintaining design control documentation
Applies basic statistical techniques and utilizes design of experiments with moderate guidance
This is a highly collaborative position and requires excellent leadership, verbal, and written communication skills
What we offer:
Flexible work arrangements allow our team members to collaborate remotely and onsite to experiment, discover, create, and simply connect with others toward a common purpose