Full Stack Developer

A clinical trials organisation is seeking a Full Stack Developer to support the design, development, and maintenance of secure, high-quality software solutions. The successful candidate will work across the full development lifecycle in a regulated environment, ensuring all work is delivered in line with SOPs, quality standards, and regulatory requirements.

This role requires a strong technical background, excellent attention to detail, and the ability to balance teamwork with independent ownership of assigned work.

This role is based at our unit in Wythenshawe, Manchester, with an option for hybrid working.

• Develop and maintain Win Forms and web-based applications and internal systems across the full stack
• Build and support APIs and related integrations
• Work within a regulated clinical trials environment, following SOPs and applicable compliance requirements
• Contribute to secure software design, development, testing, and deployment
• Maintain and improve CI/CD pipelines and deployment processes, including Jenkins
• Support observability and monitoring practices using Open Telemetry, Loki and Grafana
• Write efficient, maintainable code and support code reviews and testing activities
• Work closely with cross-functional teams including operations, QA, and stakeholders
• Take ownership of assigned tasks and manage workload effectively to meet deadlines
• Troubleshoot, diagnose, and resolve software issues in a timely manner
• Produce and maintain technical documentation where required

• Strong experience with C#
• Experience with .NET Framework and .NET Core
• Knowledge of Entity Framework
• Experience with API development and integration
• Working knowledge of CI/CD practices and Jenkins
• Experience with observability tools and practices, including Open Telemetry, Loki and Grafana
• Understanding of software security principles and secure coding practices
• Experience working in a team environment within an Agile or collaborative delivery model
• Ability to work independently, take responsibility for workload, and deliver to deadlines
• Experience in a clinical, healthcare, pharmaceutical, or regulated environment
• Familiarity with validation, audit readiness, and quality-controlled processes
• Exposure to documentation and change control processes

• Detail-oriented and quality-focused
• Strong communicator with a collaborative approach
• Proactive and accountable
• Able to prioritise and manage multiple tasks effectively
  
  Comfortable working in a regulated environment where process and compliance matter

At MEU you can enjoy a competitive benefits package that supports your wellbeing, growth, and financial security. We invest in our people with a market‑leading benefits package that recognises your contribution and supports your life inside and outside of work.