ARTIDIS
AFM Scientist
Houston, TX
Sponsorship not specifiedDetected 47 days ago
Data AnalysisFDA RegulatoryMedical DevicesResearchCommunicationPublic Speaking
About the role
- This position requires 100% on-site availability and approximately 50% travel within the USA.
- Duties and Responsibilities Conduct pre-clinical and clinical AFM-based research to characterize the nanomechanical of solid tumors.
- Prepare technical documentation, study reports, work instructions (WIs), and test plans in compliance with FDA regulations and ISO 13485 standards.
Responsibilities
- ARTIDIS enables professionals to design personalized cancer treatment plans tailored to individual patients' needs and desired outcomes.
- Job Purpose We are seeking an AFM Scientist to join our Application Support team.
- You will work closely with research teams, clinical partners, and customers to deliver exceptional support, training, and troubleshooting.
- Develop and refine measurement protocols, including sample preparation methods, measurement standards, and custom specimen holder design.
- Optimize and execute measurement routines both at ARTIDIS facilities and customer sites.
- Improve AFM data analysis pipelines, conduct advanced statistical analyses, and support analytical validation testing.
- Validate the performance of new devices and measurement tools on biological samples in clinical settings.
- Gather and document user requirement and feedback to guide ongoing development and product improvements.
- Maintain strong relationships with hospital partners and customers through regular site visits and workflow support.
- Skilled in technical training, application support, and tailoring AFM solutions to end-user needs.
Benefits
- About ARTIDIS ARTIDIS is a clinical-stage health-tech start-up founded in Basel, Switzerland, that has developed the first nanomechanical biomarker for cancer diagnosis and treatment optimization.
- Develop training protocols and education for internals and externals.
- Familiar with medical device operations, ISO 13485, FDA guidelines, CE Marking, and international regulatory frameworks.
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