Quality Engineer in Cary, IL at Stryker Corporation

Date Posted: 10/3/2019

Job Snapshot

Job Description

Who we are

We are a leading developer of products used to prevent hospital-acquired conditions such as ventilator-associated conditions, skin injury due to incontinence, pressure injuries, surgical site infections and healthcare worker injury across the continuum of care. From the acute care setting to the skilled nursing and long-term care setting, as well as continued care at home, we create products that make care giving easier and provide clinical outcomes. Our success is supported by a unique culture that is summed up in the phrase, “keep it personal”. It’s our way of reinforcing a focus and commitment to our employees and customers through integrity, honesty and passion.

Who we want

Goal-oriented developers. Keeping the customer and system requirements squarely in focus, people who deliver safe and robust solutions.

Collaborative partners. People who build and leverage cross-functional relationships to bring together ideas, data and insights to drive continuous improvement in functions.

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:

Responsibilities:

  • Be an engaged member of the Customer Quality Team
  • Collect, analyze and summarize data to identify cause analysis to provide in depth descriptions of manufacturing anomalies
  • Track investigations within the customer complaint and/or nonconformance workflows to identify trends
  • Compose detailed, methodical descriptions of non conformances and customer complaints through investigative technical writing
  • Create and explain data analysis through graphs, charts and pivot tables as needed
  • Communicate and articulate problems clearly to staff and team members of different technological backgrounds
  • Provide quality related support to all areas of the plant as necessary
  • Author and/or revise Standard Operating Procedures (SOP's) as required
  • Read and understand descriptions, communications, reports, tables, diagrams, directions, regulations.
  • Identify and or participate in continuous improvement processes
  • Maintain a knowledge base that is consistent with FDA regulations
  • Continually seek to learn and develop

What you need:

Basic Qualifications:

  • Bachelor’s Degree

Preferred Qualifications:

  • Bachelor’s Degree in Engineering strongly preferred
  • Experience in a cGMP regulated pharmaceutical or medical device environment desired (specifically 21CFR211 and 21CFR820)
  • Computer literate in Microsoft Word, Excel and Outlook
  • Experience with Trackwise, Minitab and familiarity with ISO 13485 and ISO 14971

Work From Home: No

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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