#1 Job Board for tech industry in Europe

  • Job offers
  • All offersPoznańJSFrontend Developer
    Frontend Developer
    JS
    Aether Biomedical Sp. z o.o.

    Frontend Developer

    Aether Biomedical Sp. z o.o.
    Poznań
    Type of work
    Full-time
    Experience
    Mid
    Employment Type
    B2B
    Operating mode
    Hybrid

    Tech stack

      JavaScript

      master

      ReactJS

      master

      Node.js

      master

      HTML

      advanced

      CSS

      advanced

      TypeScript

      advanced

      Python

      advanced

    Job description

    About us 


    Aether Biomedical is a medical robotics company focused on bio signal processing and bionic limbs for upper limb amputees. We are a growing team aiming to make a big impact on a bionic prosthesis market. We are growing fast, and so we are looking for new people that will help us to bring our products to the market. 

    To this end we are looking to hire an ambitious Front End developer to work on our connected device platform and who is willing to make a meaningful contribution and impact to help us scale and deliver our planned portfolio of projects. 



    Qualifications, Skillsets and Personality based:


    • Master’s Degree (or equivalent) in Computer Science or related

    • 3+ years of experience as a front-end developer

    • Knowledge and experience of professional medical device software

    development cycle & comfortable with a range of project management

    methodologies (sequential/waterfall, Scrum, Agile, etc.)

    • Expertise in JavaScript (React.js, Node.js), HTML, CSS, TypeScript, Python or

    other similar technologies.

    • Understanding and experience of version control and CI/CD practices

    • Understanding of good UX design for medical device applications and pride in

    developing user friendly applications

    • Experience in working on cloud-based (Azure or ideally AWS) products and

    services

    • Relevant knowledge of both Front end and Back end enterprise technologies

    and how these are applied to deliver a quality medical device application

    • Proven track record of successfully delivered medical device product/projects

    • Understanding of medical device regulations, such as ISO 13485 and MDR,

    and familiarity with FDA guidelines would be a distinct advantage.

    • Practical experience with medical device standards such as ISO 13485, ISO

    14971, IEC 62304 & IEC 62366-1 and FDA guidelines.

    • Practical experience with information security risk management in compliance

    with ISO/IEC 27005.

    • Experience with relevant information security standards and regulations:

    HIPPA, SOC2, GDPR, ISO/IEC, FDA Guidelines .

    • Experience in Developing Medical Device(s) or safety-critical systems and

    associated processes

    • Fluent spoken and written English and excellent communication skills to

    articulate project requirements, status updates, and risks to stakeholders.

    • Flexibility to adapt to changing priorities, technologies, and market dynamics in

    the fast-paced environment of a healthcare startup.

    • Ability to understand business and market needs and translate this into value

    in terms of a medical application

    • Analytical and critical thinking, with excellent problem solving skills

    • Ability to produce clear, concise, and detailed documentation

    • Excellent team player able to work independently with minimal supervision



    Key Responsibilities:


    • Working across the full lifecycle of a medical device application from

    Requirements, Specification, Coding, Risk Management, V&V and deployment

    support

    • Designing and developing of leading-edge, user focused and highly scalable

    and compliant medical device enterprise systems

    • Deriving customer requirements in a dynamic environment and translating

    feedback and requirements into detailed user stories and acceptance criteria.

    • Translating visual and interactive designs from tools such as Figma or other

    design frameworks into a customer focused frontend implementation.

    • Developing web applications for the Aether Biomedical Digital Platform

    • Working with backend developers, mobile developers and other disciplines to

    bring a medical enterprise and mobile product to market

    • Collaboration with QARA teams to develop necessary documentation for

    regulatory submissions

    • Working closely with the team members on the technology choices and critical

    decisions throughout the project lifecycle

    • Communication with team members to solve complex technical challenges

    • Stay informed about evolving regulatory requirements for medical devices and

    ensure SaMD compliance with relevant standards and regulations.

    • Apply and support others in remaining compliant with the Aether Biomedical

    Quality Management System.


    What we offer


    • Competitive remuneration package commensurate to the role and experience

    • Work on real life product support topics that improve people's lives

    • Friendly working atmosphere in a startup environment

    • Hybrid working role with flexible working start hours

    • Office in the center of Poznań (Mostowa)

    • Training budget

    • Multisport, Medicover


    Recruitment process


    • Selection of CVs

    • Interviews (Technical & non-technical)

    • Final decision