The genetic revolution is happening and igentify is here to make your DNA
accessible and actionable every day. Want to work for a better future for mankind,
improving the health and lives people all around the world? We are a strong team
working on cutting edge solutions using cutting edge technologies, to make a difference
for a better world. If your passion and heart are in the right place,
come on and join us!

Start your career at igentify

Genetic counselor
Java developer
Junior QA engineer
Frontend developer
DevOps engineer
Head of Quality & regulation

Responsibilities

• Identify and communicate genetic customer requirements and needs to
our creative and product teams.

• Advise teams to understand and analyze genetic data as it pertains to
disorders, medical recommendations, etc.

• Perform QA tests of our genetic counseling platform

• Teach and supervise customer and internal training activities

• designing and validating algorithms for genetic testing.

Required qualifications

• Master’s degree in Genetic Counseling

• 3-10 years of experience in genetic counseling, mainly in the field of
reproductive health and oncogenetics.

• Ability to understand and analyze genetic information and the implications for health

• Ability to effectively communicate medical information, test results, diagnoses, and/or
proposed treatment in a manner easily understood by the client/ product manager, etc.

• Self-motivated and self-directed

If You have

• 8+ Years as a SW developer.

• 5+ years of experience as a JAVA developer.

• 2+ years of Java development using Spring framework
(spring-boot, spring-cloud, etc..).

• Software engineering degree or equivalent /
Technological unit alumni.

• Leading experience such (Tech lead/Team lead/etc..).

• 3+ years of experience in SQL.

• Git, Maven/Gradle experience.

• Well versed with Agile Delivery Model and processes.

Nice to have

• Experience with NoSQL (such as MongoDB).

• Experience with micro-services architecture.

• Experience with docker and kubernetes.

• Experience with docker and NodeJS.

A must

• Up to 2 years of experience in QA

• Experience with test and coverage reporting and monitoring

• Experience working in an Agile/Scrum development process

an Advantage

• Experience in a medical company

• Familiarity with CI/CD: GitHub, Jenkins

• Understanding of versioning and registry tools, such as Git

• NoSQL Databases, PostgreSQL/MySQL

If You have

• at least 5 years of experience in frontend development.

• at least 3 years of experience with single page applications based on React/Vue.js/Angular.

• Leading experience such (Tech lead/Team lead/etc..).

• Proficient in modern JavaScript, HTML, and CSS.

• Experience with a state-management library.

• Well versed with Agile Delivery Model and processes.

• Strong oral and written communications skill.

• Must have good English.

• Git, npm/yarn experience.

If You have

• At least 4 years’ experience – if You have start-up experience its a huge plus

• Development capabilities in at least one of the languages Java/NodeJs.

• Experience in installations, configurations and maintenance of server technologies.

• Hands-on experience with two or more scripting languages (Powershell/Bash/Ruby/Python).

• Monitoring systems – ELK, Grafana, Prometheus, etc.

• Familiarity with CI/CD tools and version control tools (e.g Jenkins, Git, Artifactory).

• Strong customer facing capabilities (face-to-face, telephone, virtual meetings,
and otherwise) and the ability to work and interact with consumers.

Also nice to have

• Ability to manage multiple projects of varying scopes concurrently.

• Self-motivated and self-directed.
• Ability to solve problems and learn on the go.
• Requires the ability to travel
• Fluent in Hebrew and English
• Valid driver’s license.

Responsibilities

• Management of the ISO 13485 standard, CE and
FDA compliant Quality Management System for Igentify Software Medical Device

• Management of submissions and report to authorities

• Actively promote quality culture and develop an awareness of regulatory requirements.

• Management of the ISO 27001 compliant Information Security Management System (ISMS)

• Enforce compliance with privacy protection laws and regulations such as GDPR & HIPAA

Experience required

• 5+ years of experience in a Quality Management function

• 3+ years of experience in Medical Devices Quality Management Systems

• 3+ years of experience in one of the following fields (advantage to more than one):
– Software development (system architecture, coding, V&V testing)
– Information Security / ISO 27001
– Submissions to CE / FDA
– Privacy protection laws and regulations