UX UI Designer at Pharmavise Corporation Maple Grove, MN

Pharmavise Corporation; Maple Grove (MN); A distancia; USD 75.000 - 110.000; Jornada completa

Descripción de la vacante

Pharmavise Corporation is seeking a talented UX/UI Designer to create intuitive, compliant interfaces for regulated medical devices. You will lead end-to-end design from user flows to high-fidelity mockups, balancing usability with FDA/ISO 13485 and IEC 62366 requirements.

You will collaborate with Human Factors, R&D, Quality, and Regulatory teams, translate complex requirements into clear designs, and ensure data-heavy dashboards and device displays are visually consistent and user-centered.

Formación

• Bachelor's degree in a related field (HCI, Industrial Design, Biomedical Engineering, Cognitive Science) or equivalent.
• Professional UX/UI design experience in regulated medical device, biotech, or pharma software settings.
• Experience designing within FDA/ISO/IEC usability and design control frameworks.

Responsabilidades

• Lead end-to-end UX/UI design for medical device interfaces and connected systems.
• Develop user flows, wireframes, and high-fidelity mockups to communicate design intent.
• Collaborate with Human Factors, R&D, Quality, and Regulatory teams for compliance.
• Conduct user research, heuristic evaluations, and usability testing.
• Translate risk analysis into traceable design documentation per 21 CFR 820.30 and IEC 62366-1.
• Design dashboards and data-heavy interfaces and ensure visual consistency.

Conocimientos

UX/UI design

Figma

User research

Usability testing

Design systems

Regulatory UX

Cross-functional collaboration

Prototyping

Educación

Bachelor's degree in HCI/Industrial Design/Biomedical Engineering

Herramientas

Figma

Prototyping tools

HTML/CSS/JS basics

Descripción del empleo

UX UI Designer job at Pharmavise Corporation. Maple Grove, MN.

This is a remote position.

We are seeking a talented and self-driven UX/UI Designer to create intuitive, compliant, and user-focused digital experiences for regulated medical devices and life sciences applications. This role requires balancing creativity with regulatory discipline translating complex user and technical requirements into clear, safe, 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-quality, compliant interfaces that support both patient safety and business goals.

Key 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.
  

Must-Have Qualifications:

• Bachelor’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.
  

Preferred Qualifications:

• 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.
  

This is intended for inclusion in Pharmavise’s talent database to build a qualified pool of professionals for future medical device client requisitions.