Senior Director of Engineering

4 hours ago


Reston, Virginia, United States Terumo Medical Corporation Full time
Job Summary

The Senior Director of Engineering will lead and manage a team of engineers, overseeing engineering for manufacturing, sustaining, automation, process improvement, operational excellence, and molding and extrusion of high-quality medical devices within the healthcare industry.

Key Responsibilities
  • Develop and implement technical strategies that drive innovation, optimize resources, and ensure the delivery of quality products to customers.
  • Lead and manage engineering teams, ensuring that all members are working effectively and efficiently towards the goals set forth by the organization.
  • Lead the development and automation of technologies and equipment to enable improved product performance and efficiency in manufacturing.
  • Provide technical input to the execution of the Operations Roadmap process.
  • Participate in portfolio development, management, and organizational oversight of the execution of operational cost-down activities that deliver annual gross margin improvements to the product portfolios.
  • Support commercial and operational Long-Range Planning (LRP) and Business Development opportunities.
  • Collaborate closely with key stakeholders across the organization to ensure that the engineering team is aligned with the needs of the business.
Requirements
  • Strong leadership ability with extensive knowledge of compliance to ensure adherence to engineering best practices and industry standards.
  • Strong technical skills, project management, critical thinking skills, and the ability to adhere to demands of on-time completion and within budget constraints.
  • Extensive experience in the development of new and improvement of existing manufacturing processes for global Medical Devices or other highly regulated industries in accordance with global regulatory and quality standards and requirements.
  • Proven experience with the use and upscaling automation and technology in a manufacturing environment.
  • Proven track record of monitoring and maintaining compliance with engineering best practices and industry standards.
  • Experience in the application of Design for Six Sigma (DFSS), Design for Manufacturability (DFM), Design for Assembly (DFA), Lean Six Sigma principles, and tools, and concurrent engineering principles.
  • Demonstrated understanding of the cross-functional interactions needed for the development and manufacture of new products, preferably within FDA design control guidelines.
  • Effective communication skills, both verbal and written, adept at communicating technical information to both technical and non-technical audiences.
  • Ability to develop budgetary estimates and manage their execution.
Background Experiences
  • BS in Engineering or other related technical field with 15+ years in Medical Device, Pharmaceutical, or other highly regulated industry in process development and/or manufacturing implementation/improvement.
  • 10 years of proven overall experience leading engineering teams of +25 through development process for complex projects.


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