Radiation Oncology Quality Assurance Specialist
Vor 3 Tagen
At IBA Dosimetry GmbH, we are seeking a skilled Radiation Oncology Quality Assurance Specialist to join our team.
About the RoleThis is an exciting opportunity for a highly motivated and detail-oriented professional to contribute to advancing quality assurance methodologies in radiation oncology. As a key member of our team, you will play a critical role in developing solid phantoms for Plan QA and Imaging in clinical radiotherapy settings.
The ideal candidate will possess strong knowledge of radiation physics, treatment planning systems (TPS), and quality assurance methodologies. With a focus on innovation and problem-solving, you will work closely with clinicians, medical physicists, and regulatory bodies to ensure product relevance and safety.
Key Responsibilities- Phantom Development:
- Design and develop solid phantoms that replicate human tissue characteristics and meet clinical and regulatory requirements.
- Optimize the physical and radiological properties of phantoms to ensure accurate dosimetric and geometric reproduction of clinical treatment scenarios.
- Conceptualization and Innovation:
- Research and propose innovative concepts and designs for new solid phantom products or enhancements to existing models.
- Collaborate with cross-functional teams to translate clinical needs and technological advancements into viable QA solutions.
- Requirement Specification:
- Work closely with clinicians, medical physicists, and QA specialists to gather and shape requirements for solid phantoms based on clinical workflow, treatment modalities, and regulatory guidelines.
- Define performance criteria and technical specifications for new phantom designs to ensure they meet stringent clinical needs.
- Testing and Validation:
- Design and conduct clinical tests to evaluate the performance, accuracy, and reproducibility of solid phantoms in real-world radiotherapy environments.
- Perform comprehensive QA assessments, including dose distribution accuracy, machine and treatment plan validation, and error detection capabilities.
- Collaboration and Communication:
- Act as a liaison between the R&D team and clinical staff to ensure seamless integration of solid phantom products into routine QA processes.
- Present research findings, development updates, and performance results to internal stakeholders and external collaborators.
- Documentation and Compliance:
- Prepare detailed technical documentation, including product design specifications, test protocols, and validation reports.
- Ensure all developed phantoms comply with relevant regulatory standards, such as those set by the International Electrotechnical Commission (IEC) or the American Association of Physicists in Medicine (AAPM).
- Continuous Improvement:
- Monitor the latest advances in radiation therapy, treatment planning systems, and QA processes to keep the department's products at the cutting edge of technology.
- Engage in continuous improvement efforts to refine phantom designs based on clinical feedback and emerging industry trends.
We offer a competitive salary of €80,000 - €110,000 per annum, depending on experience, along with a range of benefits including 30 vacation days and opportunities for professional growth and development.
Please apply directly online with your salary expectations and start date. If you have any questions in advance, please contact us through our website.
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