Quality Assurance Engineer (Onsite)

Posted Yesterday
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Flower Mound, TX, USA
In-Office
77K-122K Annually
Entry level
Healthtech
The Role
The Quality Assurance Engineer will ensure product quality, manage nonconformance records, analyze quality data, and support audits for compliance.
Summary Generated by Built In
Work Flexibility: Onsite

Stryker is hiring a Quality Assurance Engineer for our Global Quality Operations team in Flower Mound, Texas.

This is an onsite position based in Stryker's Flower Mound office five days per week.

As the Quality Assurance Engineer, you will provide quality engineering support in quality assurance, control, and preventative activities with a focus on continuous improvement of products and processes. You will advocate and lead the execution of initiatives and projects to enhance quality performance within the business and for our customers, ensuring compliance to regulation and standards.

What You Will Do

  • Collaborate with operations and cross-functional teams to ensure product and process quality meets defined standards and specifications

  • Review and approve nonconformance and corrective/preventive action records, ensuring timely closure and effectiveness tracking

  • Analyze quality data and maintain key performance indicators to monitor trends, identify root causes, and reduce defects

  • Support change management processes by evaluating quality impact and ensuring compliance with procedures

  • Participate in internal and external audits, provide documentation, and address audit observations within required timelines

  • Conduct risk assessments and support validation activities to ensure manufacturing processes meet regulatory and quality requirements

  • Partner with engineering and commercial teams to investigate customer complaints and implement corrective actions

  • Drive initiatives to improve inspection methods, reduce nonconformances, and enhance overall product quality performance

What You Need

Required

  • Bachelor’s degree in engineering

  • Proficiency with standard computer applications

  • Strong communication, project management, and influencing skills as well as the ability to manage multiple tasks simultaneously

Preferred

  • Familiarity with quality concepts such as risk management, corrective and preventive actions, and statistical analysis

  • Knowledge of medical device regulations and standards, including ISO 13485 and Good Manufacturing Practices (GMP)

  • Experience supporting audits or interacting with regulatory agencies (FDA, MoH, TUV, etc.)

  


  • US10: $76,500 - $122,000 USD Annual

  


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.

Skills Required

  • Bachelor's degree in engineering
  • Proficiency with standard computer applications
  • Strong communication, project management, and influencing skills
  • Familiarity with quality concepts, risk management, and statistical analysis
  • Knowledge of medical device regulations and standards including ISO 13485
  • Experience supporting audits or interacting with regulatory agencies

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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