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UX UI Designer

Pharmavise Corporation โ€ข United States of America ๐Ÿ‡บ๐Ÿ‡ธ

Remote Contract

Lead end-to-end UX/UI design for medical device interfaces and digital tools. Collaborate with cross-functional teams to ensure compliance with usability and design control standards.

Responsibilities

  • Lead end-to-end UX/UI design for medical device interfaces, digital tools, and connected systems.
  • Develop user flows, wireframes, prototypes, and high-fidelity mockups that communicate design intent effectively.
  • Collaborate with Human Factors, R&D, Quality, and Regulatory teams to ensure compliance with usability and design control standards.
  • Conduct user research, heuristic evaluations, and usability testing to validate design decisions and ensure optimal 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 intuitive 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.

Requirements

  • Bachelorโ€™s degree in Human-Computer Interaction (HCI), Industrial Design, Biomedical Engineering, Cognitive Science, or a related field.
  • Professional UX/UI design experience, ideally within medical device, biotech, or pharmaceutical software environments.
  • Proven ability to design within regulated frameworks (FDA, ISO 13485, IEC 62366).
  • Strong proficiency in Figma, including component libraries, auto-layout, prototyping, and developer handoff.
  • Demonstrated portfolio showcasing data-driven interfaces, clinical tools, or device UIs.
  • Understanding of human factors engineering, usability validation, and risk-based design documentation.
  • Excellent communication skills with the ability to collaborate effectively across multidisciplinary teams.

Key Skills

  • Experience designing for embedded systems, touchscreens, or connected IoMT applications.
  • Familiarity with front-end technologies (HTML/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.

About Pharmavise Corporation

โ™ฆ๐„๐ฑ๐œ๐ž๐ฅ๐ฅ๐ž๐ง๐œ๐ž ๐ญ๐ก๐ซ๐จ๐ฎ๐ ๐ก ๐๐ฎ๐š๐ฅ๐ข๐ญ๐ฒโ™ฆ: ๐๐ก๐š๐ซ๐ฆ๐š๐ฏ๐ข๐ฌ๐ž, ๐ฒ๐จ๐ฎ๐ซ ๐ฌ๐ญ๐ซ๐š๐ญ๐ž๐ ๐ข๐œ ๐‹๐ข๐Ÿ๐ž ๐’๐œ๐ข๐ž๐ง๐œ๐ž๐ฌ, ๐‡๐ž๐š๐ฅ๐ญ๐ก๐œ๐š๐ซ๐ž ๐š๐ง๐ ๐†๐จ๐ฏ๐ž๐ซ๐ง๐ฆ๐ž๐ง๐ญ ๐ฌ๐จ๐ฅ๐ฎ๐ญ๐ข๐จ๐ง๐ฌ ๐ฉ๐š๐ซ๐ญ๐ง๐ž๐ซ. ๐—”๐—ฏ๐—ผ๐˜‚๐˜ ๐˜‚๐˜€ ๐—œ๐—ป๐—ณ๐—ผ๐—ฟ๐—บ๐—ฎ๐˜๐—ถ๐—ผ๐—ป: We provide high-quality, cost-effective people and process solutions for your Quality, Regulatory, Engineering, Clinical, and Healthcare needs. Our company mantra ๐„๐—๐‚๐„๐‹๐‹๐„๐๐‚๐„ ๐ญ๐ก๐ซ๐จ๐ฎ๐ ๐ก ๐๐”๐€๐‹๐ˆ๐“๐˜. The safety and quality of the drugs and devices produced for patients are directly related to 2 things, ๐‘๐Ž๐๐”๐’๐“ ๐๐‘๐Ž๐‚๐„๐’๐’ ๐š๐ง๐ ๐๐”๐€๐‹๐ˆ๐…๐ˆ๐„๐ƒ ๐๐„๐Ž๐๐‹๐„. ๐–๐ž ๐๐ž๐ฅ๐ข๐ฏ๐ž๐ซ ๐›๐จ๐ญ๐ก. ๐ƒ๐ข๐Ÿ๐Ÿ๐ž๐ซ๐ž๐ง๐ญ๐ข๐š๐ญ๐จ๐ซ๐ฌ: โ˜‘๐‡๐ข๐ ๐ก๐ฅ๐ฒ ๐’๐ค๐ข๐ฅ๐ฅ๐ž๐ ๐“๐ž๐š๐ฆ: Our team of experienced consultants with diverse backgrounds in life sciences, including scientists, researchers, and regulatory experts. The quality and expertise of our team significantly impact our clientโ€™s success. โ˜‘๐’๐ฉ๐ž๐œ๐ข๐š๐ฅ๐ข๐ณ๐ž๐ ๐„๐ฑ๐ฉ๐ž๐ซ๐ญ๐ข๐ฌ๐ž: We focus on specific niches within the life sciences, healthcare, and government sectors, such as pharmaceuticals, biotechnology, medical devices, regulatory affairs, medical research, and product development. This speciali

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