Post Market Quality Engineer
Stryker
This job at a glance
- Who can apply
- New grads and up to 2 years · Bachelor's degree
- Must know
- SalesStakeholder management
- Nice to have
- Statistics
- Work
- Hybrid in Redmond
- Pay
- Not stated by the employer.
- Skill demand
- Statistics33%Stakeholder management16%Sales4%of 99 similar entry-level jobs posted in the US this week
- Listed
- Oct 29, 2026 · still open
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About the Role
As a Post Market Quality Engineer, you will be responsible for continuous product and process quality improvements. This role is Hybrid/Onsite in Redmond, Washington.
Key Responsibilities
- Analyze and present post-market quality data including complaints, service reports, Q-metrics, and trending to identify continuous improvement opportunities.
- Investigate customer complaints and drive records to timely closure.
- Own and support Nonconformance (NC) and Corrective and Preventive Action (CAPA) investigations.
- Partner with customers and cross-functional teams including R&D, Regulatory Affairs, Field Service, and Sales to resolve product quality issues.
- Conduct and maintain risk analyses, document findings, and support Risk Management activities.
- Calculate failure and harm occurrence ratings using field performance data.
- Provide post-market quality input related to product safety, reliability, durability, and design performance.
- Ensure compliance with Quality System Regulations (QSRs), internal procedures, and applicable quality standards.
- Communicate product quality insights and trends to internal and external stakeholders.
Requirements & Tech Stack
- Bachelor's degree in Engineering, Science, or a related technical discipline.
- Strong analytical and problem-solving skills.
- Excellent communication and collaboration skills.
- Ability to manage multiple priorities and work effectively in a fast-paced environment.
- Demonstrated ability to learn quickly, navigate complexity, and drive results.
Preferred Qualifications
- Experience working in a regulated industry such as Medical Device, Pharmaceuticals, Aerospace, or Manufacturing.
- Knowledge of complaint handling, post-market surveillance, CAPA, and nonconformance processes.
- Experience with failure investigation methodologies including Root Cause Analysis, 8D, or similar problem-solving tools.
- Familiarity with statistical analysis techniques and data trending.
- Knowledge of ISO 13485, ISO 14971, and FDA Quality System Regulations.
- Experience developing and implementing design controls and process controls.
- Experience supporting risk management and product quality improvement initiatives.