Our teams

Quality Assurance & Regulatory Affairs

  • Quality Assurance & Regulatory Affairs in Szczecin

    #DocumentationSupervision #InternalAudits #CorrectiveActions #PreventiveActions #ProcessManagement #RegistrationOfMedicalProducts #StandardsAndRegulationsSupervision #RiskAssessment #ProjectDocumentation #RegulatoryAffairs

    • Have a real influence on the forming of a global system of quality assurance.
    • Take part in international projects and fulfil a variety of tasks.
    • Benefit from the possibility to develop your competence under expert supervision.
    • Join an international team of internal auditors.
    • Use quality assurance tools and IT systems tailored for individual needs.
    • Together we form a young, unified team which is open to new challenges.


    Regulatory Affairs Manager



    We are responsible for maintaining a global quality management system and we ensure compliance with medical device regulations.

  • Quality Department in Mierzyn

    #QualityManagement #QualityTools #QualitySystems #Certificates #QualityEngineering #Audits

    • Maintain the quality of technically advanced equipment in the entire spectrum of audiology.
    • Form an experienced quality assurance team, improve products and make production processes more efficient.
    • Take part in external audits and implement the Medical Device Single Audit Program.
    • Cooperate with specialists from Denmark, Germany, USA and Great Britain.
    • Work in a diverse environment, in a multinational, stable company.


    Quality Director



    If you want to see how the knowledge from quality assurance, electronic, mechanic and acoustic studies can be put to practical use, join our Quality Department, where you can create and manage as well as oversee the quality of products.