Senior Engineer, Product Development in Mahwah, NJ at Stryker Corporation

Date Posted: 9/23/2019

Job Snapshot

Job Description

Help Stryker Joint Replacement find and develop the next great Orthopaedic product.  This unique opportunity will draw on your product development experience and deepen your understanding of what it takes to succeed in the marketplace.  You’ll collaborate and innovate across Stryker in partnership with our most senior surgeon consultants to bring the next generation of additively manufactured robotically enabled orthopaedic products to market.

  • Primary
    • Lead objective, data driven feasibility assessments of new products opportunities in alignment with key stakeholders to assess their potential fit in the New Product Development pipeline. 
    • Build efficient Feasibility Assessment Plans which drive accountable progress toward meaningful assessment of assigned concepts.
  • Clinical understanding
    • Leverage a strong understanding of clinical orthopaedic practice derived from previous surgeon interaction, product development and operating room observation to build feasibility assessment plans along the most relevant directions.
  • Collaboration
    • Enlist the guidance of established subject matter experts so that their knowledge and experience can be leveraged to better understand the value of promising product concepts.
    • Collaborate with cross functional team members to build robust feasibility assessment plans and work with those team members to drive accountable completion of those plans.
  • Surgeon engagement
    • Build and maintain collaborative relationships with orthopaedic surgeons to solicit ideas for new product opportunities. 
    • Interact comfortably and professionally with orthopaedic surgeons to gain insight into the driving clinical needs and practical limitations associated with promising opportunities.
    • Manage surgeon expectations to align with achievable capabilities.  Maintain a pattern of integrity associated with doing what you say you will do.
  • Regulatory
    • Leverage a strong understanding of regulatory requirements to anticipate potential challenges to product concepts passing through US and international regulatory bodies. 

Minimum Qualifications

  • 2+ years of product development related experience in orthopaedics or the medical device industry.
  • Experience in design controls and risk management within a regulated industry.
  • Experience with a CAD design package.  Prefer Pro/Engineer. 
  • Demonstrated understanding of common design verification and validation practices in the medical device industry
  • Demonstrated understanding of Finite Element Analysis (FEA) and its application.

Work From Home: Yes

Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

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