India · On-site
Purpose of the job position: The Software Developer (Internal Products) is responsible for designing, building, and maintaining the web applications that make up iVigee's internal product portfolio, including our pharmac…
Skills: Next.js, Node.js, React, JavaScript, TypeScript
Capital City of Prague, Prague, Czechia · On-site
About the role This role exists to co-own iVigee's IT infrastructure and DevOps capabilities alongside the IT Director. You'll keep day-to-day operations running reliably — covering Microsoft 365, Azure, endpoint managem…
Skills: Git, CI/CD, Linux Administration, Docker, Azure
Czechia · On-site
About the role We are seeking a Pharmacovigilance Project Manager to join our team in Prague, CZ. This role ensures that client requirements are fulfilled, project deliverables are completed on time, and project team mem…
Skills: Pharmacovigilance, Project Management, JIRA, SharePoint, Stakeholder Management
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The Software Developer will design, build, and maintain internal web applications using Next.js, React, and Node.js. They will also collaborate with product leads to translate requirements into performant, secure, and maintainable software solutions.
Candidates must hold a bachelor's degree in a relevant field and possess at least 2 years of experience in production web application development. Proficiency in JavaScript, TypeScript, and relational database management is required, with experience in regulated industries being a plus.
Purpose of the job position:
The Software Developer (Internal Products) is responsible for designing, building, and maintaining the web applications that make up iVigee's internal product portfolio, including our pharmacovigilance reporting, signal management, and workflow automation platforms. This individual works across the stack, with primary depth in Next.js and Node.js, translating product requirements into well-structured, performant, and maintainable applications used daily by internal delivery teams and, increasingly, by our clients. The ideal candidate is a hands-on engineer who has shipped and supported production web applications, takes ownership of quality from design through release, writes code that colleagues can read and extend, and is eager to grow quickly in a small, fast-moving product team where sound judgement matters as much as technical skill.
MAJOR TASKS AND RESPONSIBILITIES:
Application Development and Delivery:
Technical Design and Code Quality:
Product Collaboration and Support:
Team Contribution and Continuous Improvement:
Specific requirements for the position:
Education | Bachelor's degree or higher in Computer Science, Information Technology, Software Engineering, or a closely related discipline. |
Experience | At least 2 years of hands-on software development experience building and supporting production web applications. Practical, project-level experience with Next.js and Node.js, including work that has been released to real users. Experience working with relational databases and integrating applications with external APIs and services. Prior experience in a regulated industry such as life sciences, pharmacovigilance, or healthcare is a plus. |
Special skills | Strong command of JavaScript and TypeScript, modern React patterns, and the Next.js rendering, routing, and data-fetching model. Practical experience with server-side Node.js development, REST API design, authentication, and session handling. Working knowledge of SQL and relational data modeling; exposure to Python and FastAPI is a plus. Familiarity with Git-based workflows, CI/CD pipelines, containers, and cloud hosting, with Microsoft Azure preferred. Ability to take a feature from requirement to release and work productively with light supervision. |
Language skills | Excellent English communication skills with strong command over written and spoken language. Ability to explain technical decisions and trade-offs clearly to non-technical colleagues. Ability to work independently and collaboratively in a fast-paced product environment. Detail-oriented with a strong focus on code quality, reliability, and maintainability. |
Computer skills | Excellent proficiency with modern development tooling, including Git, an IDE such as VS Code, Node-based build tooling, and API testing tools, strong working knowledge of Microsoft Office Suite (Word, Excel, PowerPoint, Outlook). |
iVigee delivers physician-led pharmacovigilance grounded in truth. You receive pharmacovigilance services and consulting across the entire product lifecycle, from clinical development through post-marketing authorization. Our approach is built on transparency, regulatory realism, and straight answers you can trust, so you’re never left guessing. You work with physicians, former regulators, EU QPPVs, and senior safety leaders who understand how pharmacovigilance is evaluated in real inspections. We focus on what regulators actually look for, what they question, and what they expect you to explain, not just what guidance says. We support you as you build, optimize, and transform your pharmacovigilance capabilities, providing clarity at every stage, from early system design through mature, inspection-ready operations. Across everything we do, you always know where you stand, before inspections, before submissions, and before issues become findings. iVigee operates under an ISO 9001: 2015 – certified quality management system, ensuring the way we work is as structured, consistent, and accountable as the systems we help you establish and maintain.
Offices: 1500 District Ave, Burlington, Massachusetts 01803, US · Hvězdova 1716, Praha 4, Prague 140 00, CZ · Čajakova 5, Košice, Kosice 040 01, SK
iVigee delivers physician-led pharmacovigilance grounded in truth. You receive pharmacovigilance services and consulting across the entire product lifecycle, from clinical development through post-marketing authorization. Our approach is built on transparency, regulatory realism, and straight answers you can trust, so you’re never left guessing. You work with physicians, former regulators, EU QPPVs, and senior safety leaders who understand how pharmacovigilance is evaluated in real inspections. We focus on what regulators actually look for, what they question, and what they expect you to explain, not just what guidance says. We support you as you build, optimize, and transform your pharmacovigilance capabilities, providing clarity at every stage, from early system design through mature, inspection-ready operations. Across everything we do, you always know where you stand, before inspections, before submissions, and before issues become findings. iVigee operates under an ISO 9001: 2015 – certified quality management system, ensuring the way we work is as structured, consistent, and accountable as the systems we help you establish and maintain.
Offices: 1500 District Ave, Burlington, Massachusetts 01803, US · Hvězdova 1716, Praha 4, Prague 140 00, CZ · Čajakova 5, Košice, Kosice 040 01, SK
