Work Flexibility: HybridPosition Summary:As a Senior Engineer, you will be part of a global team with multi-site responsibilities sustaining our world class hip and knee replacement devices (implants and instruments).
You will partner with our cross-functional colleagues (manufacturing, quality, regulatory, design assurance & clinical) to support a diversity of challenges, including; product design updates, design-for-manufacturability activities, tolerance analysis/stack-ups, prototyping, design control updates, provide training on product knowledge, regulatory body submissions, manufacturing transfers and more!Talents we are looking for:Analytical problem solvers.
Critical thinkers who are motivated to solve challenging problemsCollaborators.
Partners who listen, share thoughts, and work together to build and leverage relationships in order to meet project goalsDedicated achievers.
Those who aspire for excellence in a fast-paced environment and take ownership of their workCustomer focused.
Engineers who can partner with our customers to drive purposeful innovation, resulting in best-in-class productsSelf-starter.
Autonomous self-motivated engineers with excellent initiative and passion for delivering resultsWhat you will do:Actively participate on, and sometimes lead, cross-functional design teams to address design issues and maintain existing designs.Utilize/Manage design controls and risk management tools.Model and detail implant and instrument designs utilizing Pro/Engineer design software.Develop verification and validation protocols and technical reports.Become a subject matter expert on our JR product portfolio and deliver training to our internal partnersPartner with GQO teams in relations to Process Validation, Gauge Design & Inspection, Inspection Methodology and DFM.Interface with clinical advisors to gather input for design modifications and assessment of product risk.Utilize knowledge of the surgical procedure in order to develop innovative solutions to solve / satisfy customer needs.Collaborate with our manufacturing partners to troubleshoot and resolve challenges associated with supply of our product to the marketSupport FDA and world-wide submissions through design rationales and compliance to industry standards with an international team.What you need:B.S.
Degree in a science or engineering discipline.
Mechanical or Biomedical preferred.2+ years experience in medical device industry or other regulated industry preferred.Excellent presentation and written / verbal communication skillsExcellent organizational, interpersonal, communication and influencing skills.Ability to read detailed engineering drawings and understand basic GD&T tolerancing principles to the ASME Y14.5 (or equivalent) standard.Be a positive, energetic team player, and an advocate for product excellence and quality.Capable of working as part of a multi-disciplined team in a dynamic and results motivated environmentHigh level of PC skills.
Must be proficient with Microsoft applications (Outlook, Word, Excel, PowerPoint, etc.)
and CAD package (Creo/Pro-Engineer preferred).Travel Percentage: 10%
