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  • All offersPoznańMobileMedical Device Mobile Application Developer
    Medical Device Mobile Application Developer
    Aether Biomedical Sp. z o.o.

    Medical Device Mobile Application Developer

    Aether Biomedical Sp. z o.o.
    Type of work
    Employment Type
    Operating mode

    Tech stack



      Mobile Apps


      Amazon AWS








      React Native


    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 Mobile application 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.


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

    • Knowledge and experience of professional medical device software

    development cycle & comfortable with a range of project methodologies

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

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

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

    developing user friendly applications

    • Experience in developing native iOS, Android or cross compiled apps within a

    medical device setting

    • Experience with wireless communication protocols like Bluetooth low energy


    • Experience of working with mobile application technologies such as Flutter,

    Xamarin, React Native or equivalent technologies.

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

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


    • 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.

    • Experience with relevant information security standards and regulations:

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

    • 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 medical device 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 as a mobile app developer you be responsible for:

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

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


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

    and compliant medical device applications

    • Ability to interpret 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 applications.

    • Developing mobile applications to interface to the Aether Biomedical Zeus hand

    and Aether Biomedical Digital Platform

    • Working with front end, backend and 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