Your role:
Support the management of Nonconformances (NC), Quality Notifications (QN), and Corrective and Preventive Actions (CAPA) to maintain compliance and elevate quality performance.
Partners with operations, suppliers, and cross-functional teams (including R&D and Manufacturing) to resolve issues, implement improvements, and transfer new products into production.
Contribute to risk assessments, Process Failure Mode and Effects Analysis (PFMEA), and process validation efforts to strengthen manufacturing controls.
Monitor operational performance and prepare quality reports to highlight trends, improvements, and compliance status for stakeholders.
Develop your expertise in quality engineering practices and continuous improvement methodologies while supporting high-impact projects in a regulated manufacturing environment.
You're the right fit if:
You’ve acquired 2+ years of experience with a Bachelor’s degree, or 4+ years of experience with vocational education, in Quality Engineering, Process Engineering, or a related field.
Your skills include experience with process quality management, data analysis, root cause investigation, corrective actions (CAPA), and manufacturing processes.
You’re an excellent communicator and collaborator who thrives in cross-functional environments and is eager to grow within quality engineering and continuous improvement.
You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this .
How we work together
This is an office role.
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help improve the lives of others.
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