Senior Full Stack Developer

We are seeking a lead programmer obsessed with product and company success. We are offering competitive starting pay with the opportunity for major incentives/raises/bonuses.

Expectations are high and the selected candidate will be responsible for leading the programming department and learning/applying new skills specific to this position.

This position will inherently require that the applicant be adaptable. A thorough understanding of systems and Software Development Lifecycle (SDLC) is required.

Summary:

This role will involve assisting in the assembly of a new, small team and providing technical & social leadership. The hired individual will work closely with a dedicated regulatory professional and the founder/CEO to ensure that our software meets the relevant medical device regulations.

An initial estimate of hours is: 70% programming/design, 10% documentation, 10% team management (note, this number will grow as more members join the team), 10% allocated for continued education/training. These numbers will also change based on company needs.

Tech Stack:

The core product is programmed in SWIFT and runs on an iPad Pro 11-inch tablet using the Apple Pencil 2 Stylus.

Our backend use a combination of the following: EC2 instances with Django, Gunicorn, and Nginx; AWS cloud, Amazon RDS (PostgreSQL), S3 and Amazon CloudFront, and Heroku. Please note that some of these components might have changed in the newest release and the new team is able to restructure them.

We also utilize an admin panel website and various API/SDK’s from 3rd party apps and unrestricted open-source code.

Key Responsibilities:

Transition and Transform Current Software Prototype: Lead transition process from old software team to you and your team. Assist in creation of a small team of 2-3 core programmers.

Manage SDLC: Drive all stages of the Software Development Life Cycle (SDLC), ensuring our medical device software aligns with FDA guidelines & IEC 62304 from prototype to deployment and maintenance.

Architecture & Programming: Pragmatically develop and improve software architecture by weighing pros and cons with options (e.g., determine when we should program aspects ourselves vs. using open source, API, out of the box solutions, etc.).

Team Management: Lead our programming team and communicate with CEO when additional people are required full time or for specific contracted roles (e.g., we might hire a cybersecurity expert for 1 month of work).

Regulatory Learning: It is likely that the applicant will not have experience in all required regulatory areas. As such, it will be mandatory for candidate to learn these regulations alongside the CEO and regulatory expert on the team. The selected candidate will need to comprehend regulations and ensure all clauses are systematically designed, implemented, and verified.

Risk Management: Implement an effective risk management process that identifies and mitigates potential hazards throughout the software's lifecycle, in alignment with ISO 14971 standards. CEO & Regulatory expert will be heavily involved in this portion.

Quality Management: Establish a robust Quality Management System (QMS) per FDA's Quality System Regulation (QSR) and ISO 13485. CEO & Regulatory expert will be heavily involved in this portion.

Validation and Verification (V&V) Leadership: Direct and perform V&V activities ensuring that the software/device meet user needs, intended uses, and consistently fulfills all requirements. CEO & Regulatory expert will be heavily involved in this portion.

Design Control Procedures: Implement design controls in compliance with FDA regulations (21 CFR 820.30). CEO & Regulatory expert will be heavily involved in this portion.

Cybersecurity Governance: Address potential vulnerabilities, strategize, and oversee cybersecurity in compliance with FDA guidelines. CEO & Regulatory expert will be heavily involved in this portion.

Data Integrity and Security: Ensure robust data integrity, security, and compliance with laws like HIPAA and GDPR. CEO & Regulatory expert will be heavily involved in this portion.

Qualifications:

• Full stack programming background required.
• Clear experience and success in senior programming roles required.
• Strong English communication skills required.
• Prior experience in medical software and/or devices is recommended, but not required.
• Familiarity with regulatory standards (CFR 820, CFR 21 part 11, IEC 62304, ISO 13485, and relevant security guidelines) is beneficial, but the ability to learn and apply these regulations is also acceptable as guidance will be provided.

High intelligence required. A steep learning curve will be necessary to learn various regulations.

Pay: Rs 125,000.00 - Rs 300,000.00 per month