About ARTIDIS
ARTIDIS AG 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. The ARTIDIS nanotechnology platform integrates different types of clinical data into the ARTIDISNET digital platform, allowing physicians to significantly shorten the current diagnostic process and benefit both the patient and the healthcare system. ARTIDIS enables professionals to design personalized cancer treatment plans tailored to individual patients' needs and desired outcomes.
Job Purpose
The Application Scientist assumes a pivotal leadership role within the realm of medical device operations, leveraging their expertise and experience to propel project success. They play a crucial role in formulating and implementing operational strategies, ensuring that the product or service attains the highest caliber in terms of quality standards and regulatory compliance.
Duties and Responsibilities
Conducting pre-clinical and clinical research to characterize the nanomechanical properties of solid tumors.
Formulating innovative protocols and methodologies for sample preparation, including the establishment of measurements & tests standards and specimen holders.
Producing technical documentation, study reports, work instructions (WI), and test plans to ensure compliance with FDA regulations and ISO quality standards.
Author manuscripts, publications, and serve as a representative for the technology and scientific advancements at core conferences.
Enhancing and refining data analysis procedures, and executing statistical analyses and analytical validation tests.
Validate the performance of new measurement devices on biological samples at customer sites.
Offering scientific and technical support to clients, ensuring the optimal functionality and performance of ARTIDIS's products.
Provide support to customers and medical staff through education and training to enhance the performance of ARTIDIS products.
Qualifications
Ph.D. or equivalent in Biomedical Engineering, Materials Science, or related field.
Proven nanomechanical phenotyping experience in solid tumors.
Skilled in sample preparation protocols and standards.
A comprehensive grasp of medical device functionalities, along with expertise in relevant regulations and quality standards (such as ISO 13485 and FDA guidelines), is complemented by a thorough understanding of regulatory requirements encompassing FDA, CE Marking, and other international standards.
Proficiency in data analysis, statistics, and validation tests.
Experience in technical assistance and product performance optimization.
Track record of publishing and presenting at scientific conferences.
Strong interdisciplinary teamwork and problem-solving abilities.
Excellent written and verbal skills for technical reporting.
Efficiently handle multiple projects and meet deadlines.
Stay updated with evolving technologies and methodologies.
Adherence to high ethical standards in research and reporting.
Proven ability to work in a dynamic, fast-paced environment and meet project deadlines.
Working Conditions
The environment is a typical start-up with an intrinsically motivated international team. Our company is an excellent place for rapid advancement and offers a promising opportunity to learn and share know-how in a very agile environment. The position requires the employee to go the extra mile when needed. We are looking for a team player who appreciates direct communication. The effort is rewarded with challenging tasks, the possibility to take responsibility, a highly driven team and work serving a significant purpose. The job position comes with a competitive salary and a bonus for outstanding performance.