Associate Software Engineer - European Hours

Job Description

Are you a recent computer science graduate or have hands-on experience working with C# .NET and SQL? Would you like to apply your skills to make a positive impact on health and quality of life within the pharmaceutical industry? Do you value working creatively and independently?

If so, we are looking for a motivated Associate Software Engineer to join our Systems Engineering team and you could be our ideal candidate! This role is perfect for somebody eager to learn, contribute to real production systems and continuously develop their technical skills with the support of experienced engineers.

Key Responsibilities:

• Supporting the Systems Engineering team in the development, testing and maintenance of internal applications and services.
• Collaborating with project managers, business units and the Systems Engineering team to deliver new features, improvements, troubleshooting and debugging of issues.
• Writing clean, maintainable, test-driven and well-documented code following team standards and best practices.
• Contribute to testing, documentation and challenging development processes for continuous development.
• Provide technical support for systems within the Systems Engineering remit.

Qualifications

Required Skills and Qualifications

• Bachelor’s degree, Diploma or equivalent experience in Computer Science, Software Engineering or a related discipline.
• Demonstrable experience of full-stack development in C# .NET Framework / Core, ASP.NET MVC / Razor, HTML, CSS3 and JavaScript.
• Familiarity with software development IDEs (e.g. Visual Studio and VS Code) and version control tools (e.g. Git).
• Understanding of basic data structure and object-oriented development principles.
• Strong problem-solving skills, critical thinking skills and good attention to detail.
• Strong interpersonal skills, prioritisation skills and the ability work both independently and collaboratively.
• Enthusiasm for keeping up to date with developments in process and software engineering methods and technologies.

Desired Skills

• Experience of 1- 2 Years is preferred
• Demonstrable experience in T-SQL and SQL Server.
• Understanding and/or experience of cloud computing platforms (e.g. Azure or AWS).
• Exposure to development management tools (e.g. Azure DevOps or Jira).
• Knowledge of development methodologies (e.g. Scrum or Agile).
• Experience with workflow automation platforms (e.g. Power Automate).
• Knowledge of computerised system validation concepts.

Other Requirements

• Fluent in spoken and written English.
• Must be available to work within CET / GMT business hours.

Additional Information

When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.  

We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here. 

• Quality: we hold ourselves to the standard patients deserve. 

• Integrity and trust: we do the right thing, especially when it is hard. 

• Drive and passion: we care about the outcome, because someone is waiting on it. 

• Agility and responsiveness: we move quickly, because patients cannot wait. 

• Belonging: everyone is welcome, and every voice counts. 

• Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 

Company Description

Medicine moves forward here. So will you. 

Clinical trials, safety studies, and audits make safe and innovative pharmaceutical-led care possible. As part of Ergomed Group, you help patients benefit so they experience more of life’s meaningful moments. Biopharmaceutical companies are our clients. Patients are our purpose. 

Ergomed Group brings together Ergomed CRO, PrimeVigilance, Prudentia, and ADAMAS Consulting to help biopharmaceutical companies develop, deliver and safeguard therapies in oncology, rare disease and other complex areas of medicine. Across the Group, our teams turn the signals that clinical trials, safety systems and quality data generate into insight that helps bring safer treatments to patients around the world. 

The science and analysis that guides our work is demanding. And this is where we excel. What defines us, though, is how we work together. Across countries, cultures and time zones, we bring kindness, curiosity and a shared sense of purpose to work that genuinely matters. Ideas are welcome here. Growth is expected. And every person has room to make a real difference to patients' lives. 

Whether you are early in your career or bringing decades of experience, we want you to feel valued for what you do and for who you are. If that sounds like the place you have been looking for, we would love to hear from you.