We’re hiring!
Always on the lookout for talent, we want to hear from you.
Our open positions follow, but if you have an interest in behavior change, digital health, analytics, sensors, design or healthcare sales and marketing, please send a resume and cover letter to jobs(at)asthmapolis.com.
Supply Chain Management Specialist
Role/Responsibilities
This is your opportunity to make an impact solving big, important problems in a small but vocal team. Your primary responsibility will be designing, building and consuming RESTful web services for our disease management platform. We have a modern, but very deep, coding stack. The back-end services run on Node.js and Mongo. The client applications include native iOS and Android applications as well as multiple browser interfaces. The most successful developers will wear multiple hats as needs arise. This will include mobile and back-end development, as well as customer support. In your primary role, your responsibilities include:
- Implementing JSON-based web services.
- Implementing data analytics and finding answers inside a vast amount of data.
- Researching and experimenting with third-party data sources.
- Working in a collaborative development environment.
- Implement and follow development processes that comply with medical regulations while enabling the team to work efficiently.
About You
- You focus on creating great outcomes for your customers.
- You make the people around you smarter.
- You see learning as an opportunity rather than a roadblock.
- Architecting the client-side software for our web products.
- Implementing JSON-based web services.
- Researching and experimenting with third-party data sources.
- Working in a collaborative development environment.
- Software development using JavaScript frameworks (e.g. JQuery) .
- Implement and follow development processes that comply with medical regulations while enabling the team to work efficiently.
- You like nothing more than to delight the people that interact with your creations.
- You can carry the load of leading design choices as well as implementing the ideas of others.
- You’re efficient at implementing user experiences in HTML, CSS and Javascript.
- You enjoy collaborating with developers.
- You understand that technology, by itself, does not delight customers. That the sweet spot combines technology with practical solutions, surprises, utility and social interaction.
- You love web development so much, you do it in your spare time and not just 9-5.
- Software development on Android and/or iOS with support for multiple handsets.
- Building robust Bluetooth interfaces.
- Researching and experimenting with third-party data sources.
- Working in a collaborative development environment.
- Implementing and following development processes that comply with medical regulations while enabling the team to work efficiently.
- You’re an expert in user interface and user experience design and like nothing more than to delight the people that interact with your creations.
- You have working knowledge of one or more mobile SDKs (Android and iOS).
- Not only do you have a good understanding of what the mobile platforms are capable of, you understand their limitations and view the constraints as an opportunity rather than an obstacle.
- Ideally, you’ve used Bluetooth interfaces on at least one of the mobile platforms.
We’re looking for a talented, seasoned Interactive Designer to join our well-funded mobile health startup in Madison. It’s a great opportunity to wear many hats and have tons of influence on the look and feel of a suite of software solutions.
From concept to final production, you’ll manage interactive design at Asthmapolis. Working with other clever staff, you’ll help define and maintain a consistent look and feel to everything we do, from web and mobile product UX, to icons, and email communications.
- Create mobile-first interaction designs that are visually balanced for a variety of screen sizes and form factors (smart phones, tablets, and web).
- Foster a culture of collaboration, feedback and iteration to ultimately execute the most successful design options.
- Conceptualize, develop, and produce a range of interactive projects including desktop, iOS and Android, mobile web, banner ads, interactive campaigns and other digital solutions – and maybe even a little print.
- Develop consistent UX principles and UI guidelines that are applied to all product interfaces.
- A passion for user-centered design.
- You love pixels.
- You are both a conceptual thinker, and a detailed designer.
- You’re comfortable reviewing code with a developer to understand limitations and opportunities while prototyping.
- You understand the different requirements of graphical artifacts being used in web, mobile, and physical products.
- You want to come up with the big idea and crank out the icons to back it up.
- You prototype your ideas – from paper to HTML to Adobe – and iterate quickly given changing requirements.
- You love moving fast and motivating everyone around you to build great things.
We’d love to see your stuff, from napkin sketch to prototype to final production. Send your cover letter, resume and a link to your online portfolio to jobs(at)asthmapolis.com with “Interactive Designer” in the subject line of your email.
Supply Chain Management Specialist
We are looking for a bright, intelligent individual with integrity for an exciting role as part of our Implementation group. The Supply Chain Management Specialist will lead supply chain management at Asthmapolis.
This newly created position reflects our growth and the desire to incorporate your fresh ideas that will not only impact the presentation quality of our finished medical devices, but will also contribute to the quality of the medical device itself.
- Responsible for assisting in developing, applying and maintaining quality for finished device appearance for our exciting product line
- Coordinates all inventory management and fulfillment
- Authors and executes first article inspection protocols
- Creates quality inspection level requirements based on valid statistical rationale for incoming inspection
- Authors and executes incoming inspection protocols
- Analyzes test results and presents them for review
- Coordinates disposition of non-conforming materials, storage, and tracking
- Maintains identification and traceability and device history records
- Identifies and records problems or potential problems relating to the product and/or process for supply chain management, or the Quality Management System
This is a fantastic opportunity for the right candidate as Asthmapolis moves into a period of explosive growth while we continue the development of our commercial product line and build our internal foundation. We’d love to hear from you!
- You’re an expert in supply chain management within the medical devices industry
- You have an understanding of medical device regulations for the US FDA
- You are detail-oriented and possess superior organizational skills
- Knowledge of the 2007 European Medical Devices Directive is a plus
A bright, intelligent individual with integrity is needed for an exciting role in Quality Assurance and Regulatory Affairs in a high energy environment with rapid development cycles. This newly created position reflects our growth and the desire to incorporate your fresh ideas that will not only impact product quality before testing begins but also includes traditional testing activities that are part of device design in a regulated environment. We are looking for an inquisitive, quality-minded person to assist us in the development of some of the newest technologies being incorporated into medical devices today including cloud-based web application software, mobile software applications and wireless sensors.
The Regulatory Affairs and Quality Assurance Engineer performs verification, validation and testing of medical devices. In addition, the person in this position writes and assists in the writing of compliance process documentation, is fully engaged in regulatory submissions, performs document controls functions for the quality management system and creates and maintains design history files. This position also has a role in incoming inspection activities and in providing input for continuous improvement activities and being engaged in both internal and external audits. All of these activities are performed in accordance with the medical devices regulation, and all activities are performed in an environment intended to encourage not only revealing issues early in the process, but also in proposing solutions to the issues identified and selecting tools that assist in automating these processes.
- Responsible for assisting in developing, applying and maintaining quality for our exciting product line
- Executes software test cases designed to uncover flaws during early development
- Maintains documentation of testing for mobile applications, wireless sensors and server software applications
- Analyzes test results
- Identifies and records problems or potential problems relating to the product, process for designing the product, or the Quality Management System
- Proposes solutions to prevent the occurrence or recurrence of problems related to the product, process for designing the product or the Quality Management System
- Perform incoming inspection activities as necessary
This is a fantastic opportunity for the right candidate as Reciprocal Labs Corporation moves into a period of explosive growth as we continue the development of our commercial product line. If you are organized, detail-oriented and want to learn, we’d love to hear from you. You will be trained by several seasoned business, engineering, regulatory and quality individuals.
- Bachelor’s degree in the sciences preferred but not necessary, if we find the right person, we will train you!
- Must be detail-oriented, posses superior organizational skills and have an inherent curiosity for how devices and software function together
- Willing to learn about the Medical Devices Regulation for the US FDA (21 CFR, Part 820) and Canada (CMDR SOR/98-282), and ISO 13485 as related to Design Controls and Document Controls
- Willing to learn the 2007 European Medical Devices Directive is a plus
- Willing to learn about the types of defects that might be uncovered as part of a quality function, and how it impacts the devices that we manufacture
A bright, intelligent individual with integrity is needed for an exciting role in quality, in a high energy environment with rapid development cycles. This newly created position reflects our growth and the desire to incorporate your fresh ideas that will impact product quality before testing begins but also includes traditional documentation control activities that are part of device design in a regulated environment. We are looking for an inquisitive, quality-minded person to assist us in the development of some of the newest technologies being incorporated into medical devices today including mobile software applications and wireless sensors.
The Document Control Specialist (DCS) designs process documents that are compliant, yet pragmatic, visually appealing, but also, professional. In addition, the DCS performs the document control function for the quality management system and creates and maintains design history files. The DCS may also assist with verification, validation and testing of wireless sensors, mobile application software and cloud based software. In addition, the DCS will also have a role in providing input to the quality management system for continuous improvement activities. All of these activities are performed in accordance with the medical devices regulation, and all activities are performed in an environment intended to encourage not only revealing issues early in the process, but also in proposing solutions to the issues identified, and selecting the tools that will assist in automating these processes.
- Responsible for assisting in developing, applying and maintaining quality for our exciting product line
- Analyzes standards and incorporates the requirements into procedures and processes
- Designs process documents that contribute to compliance in the quality management system
- Maintains documentation of testing for mobile applications, wireless sensors and cloud-based software applications
- Identifies and records problems or potential problems relating to the product, process for designing the product, or the Quality Management System
- Proposes solutions to prevent the occurrence or recurrence of problems related to the product, process for designing the product or the Quality Management System
This is a fantastic opportunity for the right candidate as Reciprocal Labs Corporation moves into a period of explosive growth as we continue the development of our commercial product line. We’d love to hear from you!
- 5 years experience in technical writing for medical devices.
- Must be detail-oriented, possess superior organizational skills and have an inherent curiosity for how devices and software function together.
- Understanding of the Medical Devices Regulation for the US FDA (21 CFR, Part 820) and Canada (CMDR SOR/98-282), and ISO 13485 as related to Design Controls and Document Controls.
- Knowledge of HIPAA and PHI requirements is helpful.
- Knowledge of the European Medical Devices Directive is a plus.
- Understands the types of defects that might be uncovered as part of a quality function, and how it impacts the devices that we manufacture.
