Staff Quality Engineer

Arlington, TX - USA

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Work Flexibility: Onsite

Staff Quality Engineer

Arlington TN

This is a defined term assignment with an anticipated start date of March 2 2026and end date ofMarch 2 2027.

As a Staff Quality Engineer at Stryker youll play a critical role in ensuring our products meet the highest standards of safety and performance. Youll lead quality initiatives drive continuous improvement and influence processes that directly impact patient outcomes worldwide. If youre passionate about quality excellence and thrive in a dynamic environment this is your opportunity to make a difference.

What You Will Do

Provide oversight and direction on product and process quality performance across operations and business functions.
Lead and execute quality initiatives and projects at local and global levels to improve compliance and efficiency.
Manage internal and supplier-driven non-conformances (NCs) ensuring timely investigation and closure.
Own and coach others through Corrective and Preventive Actions (CAPAs) driving root cause analysis to completion.
Interpret and act on KPI trends to implement continuous improvement strategies.
Serve as a recognized process owner in areas such as risk management validation inspection processes and statistical sampling.
Participate in and lead internal and external audits representing quality expertise and ensuring regulatory compliance.
Support manufacturing transfers and manage product holds or potential product escapes to maintain quality standards.

What You Will Need

Required Qualifications

Bachelors Degree in Engineering Science or a related field.
4 years of experience in a Quality or Regulatory Affairs role within a regulated industry.

Preferred Qualifications

Proficiency in medical device manufacturing processes and standards (ISO 13485 GMP).
Lean Six Sigma certification or training.
Experience interacting with regulatory agencies (e.g. FDA MoH TUV).
Advanced knowledge of risk management practices CAPA audits and statistical techniques.
Familiarity with validation strategies and inspection optimization.

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 contractors legal duty to furnish information.

Required Experience:

Staff IC

Work Flexibility: OnsiteStaff Quality EngineerArlington TNThis is a defined term assignment with an anticipated start date of March 2 2026and end date ofMarch 2 2027.As a Staff Quality Engineer at Stryker youll play a critical role in ensuring our products meet the highest standards of safety and pe...

Work Flexibility: Onsite

Staff Quality Engineer

Arlington TN

This is a defined term assignment with an anticipated start date of March 2 2026and end date ofMarch 2 2027.

What You Will Do

Provide oversight and direction on product and process quality performance across operations and business functions.
Lead and execute quality initiatives and projects at local and global levels to improve compliance and efficiency.
Manage internal and supplier-driven non-conformances (NCs) ensuring timely investigation and closure.
Own and coach others through Corrective and Preventive Actions (CAPAs) driving root cause analysis to completion.
Interpret and act on KPI trends to implement continuous improvement strategies.
Serve as a recognized process owner in areas such as risk management validation inspection processes and statistical sampling.
Participate in and lead internal and external audits representing quality expertise and ensuring regulatory compliance.
Support manufacturing transfers and manage product holds or potential product escapes to maintain quality standards.

What You Will Need

Required Qualifications

Bachelors Degree in Engineering Science or a related field.
4 years of experience in a Quality or Regulatory Affairs role within a regulated industry.

Preferred Qualifications

Proficiency in medical device manufacturing processes and standards (ISO 13485 GMP).
Lean Six Sigma certification or training.
Experience interacting with regulatory agencies (e.g. FDA MoH TUV).
Advanced knowledge of risk management practices CAPA audits and statistical techniques.
Familiarity with validation strategies and inspection optimization.

Travel Percentage: 10%

Required Experience:

Staff IC

Key Skills

Computer Science
Docker
Kubernetes
Python
VMware
C/C++
Go
System Architecture
gRPC
OS Kernels
Perl
Distributed Systems

Apply Now

About Company

Stryker

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongsid ... View more

View Profile View Profile

AI AutoApply

Apply to 100+ jobs with one click