What You Can Expect

You have a key support role with significantly expanded responsibility for new product design, development, and commercialization; and/or to maintain in the market innovative medical device products in order to further Zimmer Biomet's mission and grow Zimmer Biomet's market leadership position.

How You'll Create Impact

Identifies user needs through engagement with product users (often Orthopedic Surgeons) and observation of similar device usage

Translates targeted user needs into design requirements/inputs

Creates product designs which fully address targeted user needs/requirements, and authors design rationale to document basis of all design features

Prepares and reviews information for invention disclosures and patents

Initiates, provides instruction for and coordinates with support from Zimmer Biomet cross-functional team members in the production and inspection of product prototypes for preliminary evaluation; and final design verification, design validation and process validation

Creates product production specifications which appropriately account for design for manufacturability (process capability) and inspection

Identifies and documents critical to quality product features based on product intended use, design requirements, associated user risks and the design itself

Evaluates, verifies and validates product designs relative to design requirements and to reduce user risk in compliance (includes completing tolerance stack-ups, benchtop testing and executing simulated operating room cadaveric product evaluations)

Supports Zimmer Biomet Quality, Sourcing and Manufacturing teams with new product design transfer tasks for production of market release quantities

Develops new test methods and/or predictive modeling as required to evaluate new products, and complete test method validation

Authors, reviews, presents and obtains cross-functional team member approval of design control and risk management documentation

Supports Regulatory Affairs team with the creation of new product regulatory submission documentation, preparation of materials for and conducting pre-submission question regulatory meetings

Supports clinical affairs in the creation of clinical study plans and protocols for both new and market released products for regulatory submission and post-market surveillance

What Makes You Stand Out

• Demonstrated good written and verbal communication skills, able to deliver professional communications to a global audience base
• Design for Six Sigma experience desired
• Parametric CAD modeling experience preferred; SolidEdge Software Proficiency desired
• Finite element analysis predicative modeling experience desired
• Microsoft Office Suite software proficiency required
• Demonstrated product design and development execution with a multi-disciplinary project team from user need identification/concept ideation through commercialization desired; medical device particularly orthopedic implant and instrument product design desired
• Working knowledge of ASME GD&T standards with application to product design required
• Demonstrated understanding of various manufacturing processes (including subtractive machining, anodization, additive manufacturing, forging, casting, plastic molding) and material science for application in new product development
• FDA QSR and EU MDR medical device regulatory requirements, and industry/regulatory body recognized technical product standards knowledge required; global medical device regulatory requirements knowledge preferred
• Demonstrated working knowledge of statistics with application to sample size determination, design of experiments and null hypothesis testing preferred; Minitab experience desired
• Ansys Software proficiency desired

Your Background

• Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Aerospace Engineering or Aeronautical Engineering.
• 3 to 5 years of full-time (including relevant ZB Coop/Intern) engineering experience.
• Must have experience within Medical Device

Physical Requirements

Travel Expectations

Up to 5%