Stryker Corporation

Senior Quality Engineer (Onsite)

Stryker Corporation$85K — $142K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering, science, or related discipline.
  • Minimum 2 years of experience in quality engineering or manufacturing.
  • Experience in a regulated environment with knowledge of Good Manufacturing Practices.
  • Preferred: 3 years in medical device manufacturing or quality engineering.
  • Preferred: Master's degree or quality certification (e.g., CQE, CRE).
  • Preferred: Six Sigma Green Belt or Black Belt certification.
  • Preferred: Knowledge of international medical device regulations (e.g., ISO 13485).

Responsibilities

  • Collaborate with operations and teams to enhance product and process quality using KPIs.
  • Manage non-conformances and corrective actions, ensuring timely investigations and resolutions.
  • Oversee non-conforming product processes and initiate quality records.
  • Independently execute workstreams while coordinating with teams on project deliverables.
  • Evaluate and approve change requests and validation activities in manufacturing and supply.
  • Assist in audits by providing data and expertise for compliance checks.
  • Utilize statistical methods to analyze variation and improve manufacturing outcomes.
  • Support process validation, inspection development, and risk management initiatives.

Benefits

  • Onsite work environment in Ventura, California, fostering collaboration.
  • Opportunity to work on innovative patient-specific medical devices.
  • Career growth potential within a leading company in medical technology.
  • Access to professional development resources and potential certifications.
  • Cross-functional collaboration enhancing teamwork and broadening experience.
Full Job Description
Work Flexibility: Onsite

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

As the Senior Quality Engineer, you will join a manufacturing site focused on patient-specific medical devices where quality engineering plays a critical role in maintaining process integrity and product performance. This position supports the development, manufacturing, and continuous improvement of custom temporomandibular joint prostheses in a regulated environment. You will work cross-functionally to drive quality outcomes, ensure compliance, and support operational excellence.

This role operates within a highly regulated manufacturing environment producing patient-specific implants and requires close coordination with internal teams and suppliers to meet quality, compliance, and production objectives.

What you will do
  • Partner with operations and cross-functional teams to monitor and improve product and process quality performance using defined KPIs and trend analysis.
  • Own non-conformances and corrective and preventive actions, ensuring root cause investigation and closure within established timelines.
  • Disposition non-conforming product in material review processes and initiate quality records as required.
  • Execute workstreams independently to meet defined project timelines, while coordinating with cross-functional partners to align on deliverables and support project execution as needed.
  • Evaluate and approve manufacturing and supplier change requests, including production part approval processes and validation activities.
  • Support audits (internal and external) by providing documentation, data, and subject matter expertise to demonstrate compliance.
  • Apply statistical methods and process controls to assess variation, improve capability, and maintain consistent manufacturing outcomes.
  • Contribute to process validation, inspection method development, and risk management activities to ensure compliant and robust operations.


What you need

Required
  • Bachelor's degree in engineering, science, or related discipline.
  • Minimum 2 years of experience in quality engineering, manufacturing, or related field.
  • Experience working in a regulated environment with knowledge of Good Manufacturing Practices.


Preferred
  • Minimum 3 years of experience in medical device manufacturing or quality engineering.
  • Master's degree or professional certification (e.g., Certified Quality Engineer or Certified Reliability Engineer).
  • Six Sigma Green Belt or Black Belt certification.
  • Knowledge of international medical device regulations and standards (e.g., ISO 13485).


  • US10: $85,500 - $142,500 USD Annual


Travel Percentage: 10%

About Stryker Corporation

Stryker Networks is a premier Information Technology partner providing IT managed services and database application development.

Stryker Corporation Careers

Joining Stryker Corporation means becoming part of a global team recognized for its commitment to innovation, leadership, and enhancing patient outcomes. As a leading medical technology company, Stryker is the perfect place to build a career that truly makes a difference.

Work You’ll Do

At Stryker, every position contributes to our mission of making healthcare better. Here, you will use your skills to work on transformative projects that improve lives across the globe. You will be part of a culture that thrives on growth, innovation, and leadership, and you will work alongside some of the brightest minds in the industry.

Innovative Careers

Stryker offers a range of job opportunities, from internships that provide a stepping stone into high-impact roles to leadership positions that drive strategic direction. Our team members benefit from a work environment that supports professional growth and diversity training, ensuring everyone, regardless of background, can thrive.

Be Part of a Great Team

Our employees enjoy a collaborative atmosphere that fosters innovation and encourages professional development. With a commitment to leadership and diversity, Stryker ensures that all team members have the opportunity to grow and influence the company's future. Our global scale and dedication to impactful solutions make us leaders in medical technology.

Future-Proof Your Career

Stryker is dedicated to career development, offering extensive training, benefits, and resources to help you advance professionally. From networking opportunities to workshops on resume and interview skills, we support your journey every step of the way. Our career paths are as diverse as the innovative products we develop and the markets we serve.

Explore Job Opportunities

Whether you’re just starting out or looking to take your career to the next level, Stryker provides the tools and resources to achieve your goals. We are continuously hiring and looking for ambitious, curious, and driven individuals to join our team.

Stryker Corporation – A Leader in Medical Technology

Our commitment to improving healthcare through innovative products sets us apart in the medical technology field. The synergy of our team’s expertise and our leadership in technology solutions enables us to meet the needs of our customers effectively.

Stay Connected

Join Our Team Search open positions that match your skills and interest. We look for passionate, creative, and solution-driven team players. Explore the many benefits of employment at Stryker, a company that values innovation and leadership.

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Stryker Corporation – Where Talent Meets Opportunity

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Learn more about Stryker Corporation
Size
46,000 employees
Market Cap
$91.9 billion
Industry
Net Income
$1.5 billion
Founded
2004
5 Year Trend
+8.6%
Revenue
$14.3 billion
NASDAQ

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