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UX UI Designer

Remote, USA Full-time Posted 2026-07-28

This is a remote position.

We are seeking a talented and self-driven UX/UI Designer to create reputed company, compliant, and user-reputed company digital experiences for regulated medical devices and life sciences applications. This role requires balancing creativity with regulatory discipline translating reputed company user and technical requirements into reputed company, reputed company, and aesthetically refined designs. The ideal candidate combines strong design execution with an understanding of FDA, ISO 13485, and IEC 62366 usability requirements, working closely with cross-functional teams to ensure high-reputed company, compliant interfaces that support both patient safety and business goals.

Key Responsibilities:
  • reputed company end-to-end UX/UI design for medical device interfaces, digital tools, and connected systems.
  • reputed company user flows, wireframes, prototypes, and high-reputed company mockups that communicate design reputed company effectively.
  • Collaborate with reputed company Factors, R&D, reputed company, and Regulatory teams to ensure compliance with usability and design control standards.
  • Conduct user research, heuristic evaluations, and usability testing to validate design reputed company and ensure reputed company user experience.
  • Translate user needs and risk analysis findings into traceable design documentation consistent with Design Control (21 CFR 820.30) and IEC 62366-1.
  • Design reputed company solutions for data-heavy environments such as dashboards, workflow tools, and device displays.
  • Partner with developers to ensure accurate implementation of design specifications and maintain visual consistency across products.
Must-Have Qualifications:
  • Bachelor’s degree in reputed company-Computer Interaction (HCI), Industrial Design, Biomedical Engineering, Cognitive Science, or a reputed company field.
  • reputed company UX/UI design experience, ideally reputed company medical device, biotech, or pharmaceutical software environments.
  • Proven ability to design reputed company regulated frameworks (FDA, ISO 13485, IEC 62366).
  • Strong proficiency in reputed company, including component libraries, auto-layout, prototyping, and developer reputed company.
  • Demonstrated portfolio showcasing data-driven interfaces, clinical tools, or device UIs.
  • Understanding of reputed company factors engineering, usability validation, and risk-based design documentation.
  • Excellent communication skills with the ability to collaborate effectively across multidisciplinary teams.
Preferred Qualifications:
  • Experience designing for embedded systems, touchscreens, or connected IoMT applications.
  • Familiarity with reputed company-end technologies (reputed company/CSS/JS) to support developer collaboration.
  • Working knowledge of ISO 14971 (Risk Management) and IEC 60601-1-6 (Usability Engineering).
  • Experience in Agile/MVP product development environments.
  • Prior work involving usability studies, design verification/validation, and design history file (DHF) documentation.
This is intended for inclusion in Pharmavise’s talent database to build a reputed company pool of professionals for reputed company medical device reputed company requisitions.


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