Principal Engineer

What will you do:

Technical Responsibilities:

• Lead technical team members in research, design, development, modification and evaluation of modules, assemblies, or subsystems

• Apply advanced engineering theories, principles, and concepts across various products within business

• Translate user needs to design inputs/ specifications and produce system/architectural level layouts and platform designs

• Assess new technologies and capabilities (prototyping, testing, et.al.) for the organization
  

Med Device Compliance:

• Divisional expert with extensive experience applying industry standards for device development

• Lead the development of standards and regulations, working closely with functions within and across business

General Responsibilities:

• Lead cooperative efforts with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success

• Lead and support team members to create or improve procedures, policies, processes, systems, and technology requirements

• Hold team accountable to deliver high quality results with passion, energy and drive to meet business priorities

• Mentor, develop and influence across business, intentionally building divisional relationships
  

What will you need:

Minimum Qualifications:

• Bachelor of Science in Engineering, Mechanical Engineering or Bio Medical & 13+ years of work experience

• Broad base of experience in Implementing design methodologies such as DFM, Reliability, Systems Design

• High degree of experience in medical device design (or designing in a highly regulated industry) and ability to utilize Solid Modeling and CAE tools to optimize the design

• In-depth knowledge of materials, manufacturing and processing methods and technologies to support complex product development

• Ability to communicate complex plans and technical information to team members within and across businesses

Preferred Qualifications:

• Communication skills

• Ability to lead and manage