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Strong employer brand, metro location, generalist senior fullstack title, and broad tech requirements increase competition.
Core fullstack skills are transferable, but REMS/GxP regulatory experience increases domain specificity.
Explicit 7+ years, mandatory tech stack, and regulated GxP validation requirements raise selection strictness.
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Design, build, and enhance full-stack applications primarily for risk minimization of IMiDs and CELMoDs drugs within a highly regulated life-sciences environment.
Develop scalable, secure cloud-native solutions using Java, Spring Boot, ReactJS, PostgreSQL, microservices, containerization, and BPM platforms like Camunda.
Collaborate globally with Product Managers, Architects, Test and QA teams; own code quality, compliance, deployment automation, and provide technical guidance to junior developers.
7+ years of hands-on full stack software development experience.
Strong technical skills in Java, Spring Boot, ReactJS, PostgreSQL/MySQL/Oracle, AWS (Lambda, RDS, API Gateway, ECS, S3, IAM), CI/CD tools (Jenkins/GitHub Actions/Bitbucket), BPM platforms (Camunda or equivalent).
Bachelor's or Master's degree in computer science, engineering, or closely related technical field.
Ability to work in a highly regulated life-sciences environment with compliance to SDLC, validation, and data integrity standards.
Experienced in building microservices and event-driven architectures in cloud environments with containerization (Docker) and modern software engineering practices.
Comfortable working collaboratively in global Agile teams with distributed stakeholders including Product, QA, and Risk Management.
Familiarity with Risk Evaluation & Mitigation Strategy (REMS), pharmacovigilance, or regulated patient safety domains is a distinct advantage.