Senior Design Assurance Engineer in Fort Lauderdale, FL at Stryker Corporation

Date Posted: 6/30/2020

Job Snapshot

Job Description

It's time to join Stryker!

We are a great place to work! Fortune, in association with Great Place to Work, named us among the World’s Best Workplaces. We ranked #8 out of the 25 companies on the list. This list highlights companies that have gone above and beyond to create a great workplace for employees all over the world.

Fortune also named us one of the 100 Best Companies to Work For in the United States. This is the ninth consecutive year we have been on the list, and we ranked #11 out of 100!

What We Do:

Stryker is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. At the Florida location, we are home to about 400 employees who are involved with the design and manufacture of our Robotic-Arm Assisted Surgery product which enables surgeons to have a more predictable surgical experience when performing joint replacements.

We are currently seeking a Senior Design Assurance Engineer located near Ft. Lauderdale, Florida

Who We Want:

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.

Strategic thinkers. People who enjoy analyzing data or trends for the purposes of planning, forecasting, advising, budgeting, reporting, or sales opportunities.

Analytical problem solvers. People who go beyond just fixing to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.

What You Will Do:

  • You will support the design, development and manufacturing of robotic systems, software and instruments.
  • You will develop Quality Assurance Plans for new products.
  • You will lead risk management activities for robotics by developing risk management plans/reports, conducting risk reviews, verifying implementation and effectiveness of risk controls and driving post market activities.
  • You will partnering with engineering to define design verification and validation test requirements that will ensure appropriate objective evidence is available to support the acceptance criteria. You will promote efficient testing practices.
  • You will complete or contribute to the completion of final design verification and design validation test reports by providing clear concise conclusions with statistical validity and graphical support when necessary.
  • You will utilize standard statistical analysis and problem solving techniques as necessary to determine product acceptance limits, establish process parameters, resolve quality problems.
  • You will identify supplier assessment requirements and communicate these to the supplier quality group.
  • You will evaluate product design changes for verification and validation requirements and assist in change implementation.

What You Need:

Basic Qualifications:

  • Bachelor’s Degree
  • Minimum 2 years of experience in a regulated design environment

Preferred Qualifications:

  • Bachelor's Degree in Engineering or related.
  • CQE certification and Six Sigma Green or Black Belt preferred.
  • 2+ years of experience as a Quality Engineer (QE) in a regulated design environment.  Prefer experience with medical device product development life cycle, including risk management and design/ process verification & validation
  • Knowledge of FDA QSRs, ISO 13485 Design Control Procedures and ISO 14971
  • Demonstrated applied knowledge of Advanced Quality tools such as Failure Modes Effect Analysis (FMEA), GD&T, Root Cause Analysis, and Mistake Proofing/Poka Yoke.
  • Demonstrated ability to read and interpret CAD drawings
  • Demonstrated ability to advocate product excellence and quality
  • Demonstrated ability to effectively work cross functionally with other departments including Advanced Operations, Product Development, Regulatory and Marketing.
  • Demonstrated problem-solving and troubleshooting skills.

Why Stryker?  “It’s the people.” That’s the answer you’ll hear most often when you ask our employees why they love working here. Come join our team in Davie / Ft. Lauderdale at Stryker!

Work From Home: Occasional

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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