Associate Quality Engineer
SI-BONE, IncSanta Clara, California, United States
Posted February 19, 2026
89000 - 100000 USD
Full Time
About the Company
SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions.
Job Description
SI-BONE is a fast-growing, publicly traded medical device company that is an industry pioneer in minimally invasive sacropelvic solutions. We are seeking an Associate Quality Engineer to provide Quality Department support for SI-BONE products, ensuring compliance with federal law and applicable standards. The ideal candidate will have a Bachelor’s degree in engineering or technical science and 3+ years of directly relevant experience with experience in FDA/cGMP or other regulated environment(s).
Requirements
- Investigate and review SI-BONE medical device complaints to help identify root causes, solutions, and trends
- Perform all duties in compliance with all applicable worldwide regulatory requirements as included in the scope of the SI-BONE Quality Manual
- Write protocols and reports for activities such as sterilization validation, cleaning validation, biocompatibility testing, and packaging validation for New Product Development
Benefits
- Bonus
- Stock
