Company Description
LVIS Corporation is on a mission to revolutionize the entire continuum of neurological care by developing AI driven software tools to help physicians accelerate patient throughput and improve patient diagnostic and treatment outcomes. We have an international team with our headquarters located in Palo Alto, California, USA, and we have an office in Gangnam, Seoul, South Korea. We are looking for talented individuals to join us in our mission to transform the neurology health care industry.
Responsibilities
- As our technical expert you will be responsible for the architecture and commercialization of our products in addition to service launches and operations of our Engineering Team.
- Lead and manage the technical aspects of SaMD product development, ensuring that products meet the highest quality standards and comply with regulatory requirements.
- Develop and implement software development processes and methodologies that enable efficient and effective product development.
- Collaborating with cross-functional teams, including software engineers, data scientists, and medical professionals, to design and develop innovative software solutions that improve patient outcomes.
- Establishment and execution of a mid- to long-term technical roadmap based on the company’s strategic direction.
- Work closely with Regulatory Affairs to ensure compliance with relevant regulations and standards, such as FDA guidelines and ISO 13485.
- Stay up-to-date with the latest trends and developments in software engineering and medical technology, and identify opportunities to integrate new technologies and methodologies into our products.
- Manage and mentor a team of software engineers, providing guidance and support to ensure that projects are completed on time and to the highest quality standards.
Basic Qualifications
- 15+ years of experience in software product development combined as an individual contributor and leadership.
- Must be a hands on coder.
- (Ideally) Experience developing SaMD products and knowledge of regulatory requirements for SaMD products (e.g., FDA guidelines, ISO 13485).
- Strong familiarity with our programming background - JavaScript (Vue.js, Three.js,), React, Typescript, Redux, Java (Spring Framework, Hibernate), RDBMS, and No-SQL.
- Expert level knowledge of software development processes and methodologies, including Agile and DevOps.
- Experience with successful launches of complex engineering products.
- Leading projects and teams, with the ability to manage multiple priorities and deadlines.
- Excellent communication and collaboration skills, with the ability to work effectively with cross-functional teams.
- Strong strategic thinking and problem-solving skills, with a demonstrated ability to identify and solve complex technical challenges.
- BS degree in Computer Science, Electrical Engineering, or similar technical field
