Chemical Engineer
Listed on 2026-08-26
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Engineering
Process Engineer, Quality Engineering, Biomedical Engineer
Chemical Engineer (Finance)
Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.
Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.
Siemens Healthineers is looking for a Chemical Engineer to join our interventional oncology (IO) development team. The individual will be a member of our growing embolics team that is focused on treating cancers by delivery internal chemical/radiation therapy and occluding the blood supply to tumors. The individual would contribute by developing new implantable therapy and embolization products, new applications for existing microspheres, and maintaining our existing microsphere products.
The ideal candidate would be a self-driven individual with a passion for medical device development and a desire to work on products that changes people's lives.
- Develop and define glass, ceramic, and polymer microsphere formulations and synthesis methods to meet device needs
- Develop prototype intravascular devices to demonstrate technical feasibility
- Understand, operate, and design various thermal spray processes.
- Incorporate homogenization for consistency of batches.
- Utilization of high temperature furnaces.
- Interpretation of material characterization data.
- Transfer knowledge of synthesis processes to manufacturing for ongoing production
- Development and execution of complex test plans involving significant data collection and interpretation, assessment of results, and incorporation of step for continuous design improvements
- Contribute to formal design and instrumentation drawings, analysis plans, and fabrication plans
- Plan and conduct R&D activities to define and develop implantable devices
- Quality assurance testing of devices to ensure conformance to design specifications
- Write technical documentation including process descriptions and test methods
- Contribute to and maintain FDA compliant Design History Files (DHF)
- Execute process improvements as they relate to quality system compliance with FDA 510(k), QSR and ISO 13485
- Participate in complaint investigations, and failure analysis of products
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