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"Design is where science and art break even."
โ Robin Mathew
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
- Bachelorโs 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
โฆ๐๐ฑ๐๐๐ฅ๐ฅ๐๐ง๐๐ ๐ญ๐ก๐ซ๐จ๐ฎ๐ ๐ก ๐๐ฎ๐๐ฅ๐ข๐ญ๐ฒโฆ: ๐๐ก๐๐ซ๐ฆ๐๐ฏ๐ข๐ฌ๐, ๐ฒ๐จ๐ฎ๐ซ ๐ฌ๐ญ๐ซ๐๐ญ๐๐ ๐ข๐ ๐๐ข๐๐ ๐๐๐ข๐๐ง๐๐๐ฌ, ๐๐๐๐ฅ๐ญ๐ก๐๐๐ซ๐ ๐๐ง๐ ๐๐จ๐ฏ๐๐ซ๐ง๐ฆ๐๐ง๐ญ ๐ฌ๐จ๐ฅ๐ฎ๐ญ๐ข๐จ๐ง๐ฌ ๐ฉ๐๐ซ๐ญ๐ง๐๐ซ. ๐๐ฏ๐ผ๐๐ ๐๐ ๐๐ป๐ณ๐ผ๐ฟ๐บ๐ฎ๐๐ถ๐ผ๐ป: We provide high-quality, cost-effective people and process solutions for your Quality, Regulatory, Engineering, Clinical, and Healthcare needs. Our company mantra ๐๐๐๐๐๐๐๐๐๐ ๐ญ๐ก๐ซ๐จ๐ฎ๐ ๐ก ๐๐๐๐๐๐๐. The safety and quality of the drugs and devices produced for patients are directly related to 2 things, ๐๐๐๐๐๐ ๐๐๐๐๐๐๐ ๐๐ง๐ ๐๐๐๐๐๐ ๐๐๐ ๐๐๐๐๐๐. ๐๐ ๐๐๐ฅ๐ข๐ฏ๐๐ซ ๐๐จ๐ญ๐ก. ๐๐ข๐๐๐๐ซ๐๐ง๐ญ๐ข๐๐ญ๐จ๐ซ๐ฌ: โ๐๐ข๐ ๐ก๐ฅ๐ฒ ๐๐ค๐ข๐ฅ๐ฅ๐๐ ๐๐๐๐ฆ: 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 clientโs success. โ๐๐ฉ๐๐๐ข๐๐ฅ๐ข๐ณ๐๐ ๐๐ฑ๐ฉ๐๐ซ๐ญ๐ข๐ฌ๐: 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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