More jobs:
Senior Engineer, Advanced Quality Engineering
Job in
Tempe, Maricopa County, Arizona, 85285, USA
Listed on 2025-12-29
Listing for:
Stryker
Part Time
position Listed on 2025-12-29
Job specializations:
-
Engineering
Quality Engineering, Biomedical Engineer -
Quality Assurance - QA/QC
Quality Engineering
Job Description & How to Apply Below
Senior Engineer, Advanced Quality Engineering
Stryker is hiring a Senior Engineer, Advanced Quality, for our Sustainability Solutions team supporting our reprocessing product line. In this role, you’ll be part of a team that ensures innovative medical devices are safe, effective, and compliant. You’ll collaborate across R&D, Regulatory Affairs, and Operations to deliver products that improve patient outcomes worldwide. If you’re passionate about quality and innovation, this is your chance to make a real impact.
WorkFlexibility
- Hybrid; must reside within a commutable distance to Tempe, AZ and be onsite at least 3 days per week.
- Represent Quality Assurance on cross-functional New Product Development teams to meet project milestones.
- Lead Risk Management activities, including creating and maintaining Risk Management Files and ensuring compliance with design control procedures.
- Plan, design, and implement inspection and testing methods using advanced statistical techniques to ensure product reliability.
- Conduct and lead Design Reviews to confirm design robustness and regulatory compliance (QSR, ISO 13485).
- Perform and review engineering risk analyses, test methods, and process improvements to enhance quality and efficiency.
- Guide product development by interpreting test data and developing protocols for processes and products.
- Mentor junior team members and lead departmental initiatives to drive quality and compliance.
- Collaborate with internal teams and customers to address product quality concerns and support continuous improvement.
Required Qualifications
- Bachelor’s degree in Mechanical, Electrical, Chemical, Material Science, Biomedical Engineering or related field
- 2+ years of experience in an engineering role.
- Experience in data collection, data analysis, and applying scientific methods.
- Experience with Quality concepts such as Risk Management, CAPA, Audits, and Statistics.
- Previous experience in the medical device industry.
- Knowledge of U.S. and international medical device regulations, including ISO 13485, GDP, and GMP.
- Six Sigma Green Belt or ASQ Certified Quality Engineer (CQE).
Position Requirements
10+ Years
work experience
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