In this role, you will help design, maintain, and continuously improve a quality management system that supports regulatory approval and business growth across global markets
Job Summary
In this role, you will help design, maintain, and continuously improve a quality management system that supports regulatory approval and business growth across global markets.
You’ll collaborate across functions to ensure quality processes are not only compliant, but practical, efficient, and future‑ready.
Stryker Corporation is an equal opportunity employer committed to non-discrimination and providing consideration without regard to protected statuses.
Matching Summary
In this role, you will help design, maintain, and continuously improve a quality management system that supports regulatory approval and business growth across global markets.
Skills & Requirements
Must-have
Quality management system compliance
Regulatory approval support
Quality process continuous improvement
Quality system audits preparation
Hybrid work onsite several times per week
Nice-to-have
Knowledge of U.S. and international medical device regulations
Experience with quality planning and corrective actions
Exposure to good manufacturing and distribution practices
Data-driven quality governance support
Key Requirements
Bachelor’s degree in science, engineering, business, or related discipline
0+ years experience in regulated industry
Ability to reside within commutable distance to Portage, MI