As our Data Platform Engineer - Full Stack (permanent role/ Full-time/ on-site) , you will play a key role in transforming data into life-changing medical solutions. Your mission is to design, build, automate, and maintain Debiopharm’s core data platforms, enabling seamless data management, analytics, and statistical computing company-wide. In this high-impact role, you will own global platforms end-to-end within a GxP environment, engineering secure, cloud-native solutions on Azure and AWS. Fully accountable for platform security, reliability, and automation, you will progressively step into System Owner responsibilities. You will also stay close to the business by acting as the trusted first line of support for daily user needs and L2 troubleshooting. Your Key Responsibilities Software & Platform Engineering Design, write and ship production-grade frontend & backend code for automation, integrations and internal tooling (JavaScript/Typescript/Svelte, C#, Python, Go, PowerShell, REST APIs). CI/CD on Azure DevOps: deployment pipelines, version control, testing, review, deployment, documentation. Maintain Infrastructure as Code (Terraform / Bicep) as the single source of truth for all our environments. Design and implement the platforms with strong software engineering fundamentals (following standard patterns, security and clean - maintainable code), to improve operational efficiency and developer productivity (use of AI assistance coding is encouraged but always with manual review and human in the loop).Clinical Data & Analytics Maintain & support new releases for our central data repository, and the data pipelines feeding the analytical solutions from Medidata and other clinical sources. Collaborate with Data Management, Biostatistics and Data Science teams to optimize data architecture, data quality and analytics platform capabilities. SAS Viya & Medidata Platforms Own SAS Viya 4 on Kubernetes (AKS): automate deployment, upgrades and provisioning, and become the technical reference. Act as system owner and administrator for Medidata: user access, configuration, releases and vendor coordination. Keep both platforms available, performant and qualified, under GxP change control. Cloud, Security & Compliance Implement platform observability through monitoring, logging, alerting, and performance management. Run cloud workloads secure by default and cost-aware, strengthening security posture (Defender for Cloud / CNAPP) and FinOps discipline. Follow the applicable SOPs and provide CSV documentation (IQ, OQ, etc.) for the platforms you own, with the CSV / GxP function. RequirementsYour profile Education & Certifications: Bachelor's or master's degree in computer science, Software Engineering or a related field, or equivalent experience. Cloud certifications (Azure, AWS, CKA/CKAD) are an asset; willingness to pursue them is expected. Strong experience in Kubernetes/container orchestration is a plus Technical Experience: 5+ years of software engineering (frontend and backend), infrastructure experience delivering production systems, clean code, testing, CI/CD (Azure DevOps) and AI-assisted development. Infrastructure as Code (Terraform / Bicep) and cloud (Azure and/or AWS) with solution design; production Kubernetes (AKS or EKS) is a strong asset. Databases and data engineering (SQL, data modelling, pipelines) for clinical and analytics data. SAS Viya 4 and Medidata (Rave) administration are a plus, not a prerequisite: a strong engineer will ramp up and take full ownership. Regulated / GxP and CSV exposure (documentation, change control, audit trail) is a strong asset; pharma or life sciences background welcome. Soft Skills & Mindset: Engineer at heart, thinks in code, with strong ownership and accountability for business-critical platforms. Balances engineering pragmatism with compliance requirements in regulated environments and communicates clearly with IT and business stakeholders. Continuously improves systems through automation and simplification, working across engineering, platform operations, cloud infrastructure and stakeholder engagement. Language & Location: Fluent English and good level of French Based at our Lausanne headquarters: the candidate must live in the region or be willing to relocate. BenefitsWhat we Offer: Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day Partner with teams across disciplines, at the forefront of oncology and anti-infective development An inclusive and respectful workplace — proud to be Equal-Pay certified Grow in a culture that values people, purpose, and performance A chance to grow, share, and shape the future of healthcare What to Expect in the Recruitment Process: If your application is selected, you’ll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams, followed by a panel interview and reference checks. Communication is handled via Workable—check your spam folder for emails from *@outbound.workable.com. We do not accept unsolicited applications from agencies or recruiters.
As our Data Platform Engineer - Full Stack (permanent role/ Full-time/ on-site) , you will play a key role in transforming data into life-changing medical solutions. Your mission is to design, build, automate, and maintain Debiopharm’s core data platforms, enabling seamless data management, analytics, and statistical computing company-wide.
In this high-impact role, you will own global platforms end-to-end within a GxP environment, engineering secure, cloud-native solutions on Azure and AWS. Fully accountable for platform security, reliability, and automation, you will progressively step into System Owner responsibilities. You will also stay close to the business by acting as the trusted first line of support for daily user needs and L2 troubleshooting.
Your Key Responsibilities
Software & Platform Engineering
- Design, write and ship production-grade frontend & backend code for automation, integrations and internal tooling (JavaScript/Typescript/Svelte, C#, Python, Go, PowerShell, REST APIs).
- CI/CD on Azure DevOps: deployment pipelines, version control, testing, review, deployment, documentation.
- Maintain Infrastructure as Code (Terraform / Bicep) as the single source of truth for all our environments.
- Design and implement the platforms with strong software engineering fundamentals (following standard patterns, security and clean - maintainable code), to improve operational efficiency and developer productivity (use of AI assistance coding is encouraged but always with manual review and human in the loop).
Clinical Data & Analytics
- Maintain & support new releases for our central data repository, and the data pipelines feeding the analytical solutions from Medidata and other clinical sources.
- Collaborate with Data Management, Biostatistics and Data Science teams to optimize data architecture, data quality and analytics platform capabilities.
SAS Viya & Medidata Platforms
- Own SAS Viya 4 on Kubernetes (AKS): automate deployment, upgrades and provisioning, and become the technical reference.
- Act as system owner and administrator for Medidata: user access, configuration, releases and vendor coordination.
- Keep both platforms available, performant and qualified, under GxP change control.
Cloud, Security & Compliance
- Implement platform observability through monitoring, logging, alerting, and performance management.
- Run cloud workloads secure by default and cost-aware, strengthening security posture (Defender for Cloud / CNAPP) and FinOps discipline.
- Follow the applicable SOPs and provide CSV documentation (IQ, OQ, etc.) for the platforms you own, with the CSV / GxP function.
Requirements
Your profile
Education & Certifications:
- Bachelor's or master's degree in computer science, Software Engineering or a related field, or equivalent experience.
- Cloud certifications (Azure, AWS, CKA/CKAD) are an asset; willingness to pursue them is expected. Strong experience in Kubernetes/container orchestration is a plus
Technical Experience:
- 5+ years of software engineering (frontend and backend), infrastructure experience delivering production systems, clean code, testing, CI/CD (Azure DevOps) and AI-assisted development.
- Infrastructure as Code (Terraform / Bicep) and cloud (Azure and/or AWS) with solution design; production Kubernetes (AKS or EKS) is a strong asset.
- Databases and data engineering (SQL, data modelling, pipelines) for clinical and analytics data.
- SAS Viya 4 and Medidata (Rave) administration are a plus, not a prerequisite: a strong engineer will ramp up and take full ownership.
- Regulated / GxP and CSV exposure (documentation, change control, audit trail) is a strong asset; pharma or life sciences background welcome.
Soft Skills & Mindset:
- Engineer at heart, thinks in code, with strong ownership and accountability for business-critical platforms.
- Balances engineering pragmatism with compliance requirements in regulated environments and communicates clearly with IT and business stakeholders.
- Continuously improves systems through automation and simplification, working across engineering, platform operations, cloud infrastructure and stakeholder engagement.
Language & Location:
- Fluent English and good level of French
- Based at our Lausanne headquarters: the candidate must live in the region or be willing to relocate.
Benefits
What we Offer:
- Being part of a company where innovation, collaboration, and impact aren’t just values — they’re how we work every day
- Partner with teams across disciplines, at the forefront of oncology and anti-infective development
- An inclusive and respectful workplace — proud to be Equal-Pay certified
- Grow in a culture that values people, purpose, and performance
- A chance to grow, share, and shape the future of healthcare
What to Expect in the Recruitment Process:
If your application is selected, you’ll be invited to interviews with Talent Acquisition and the Hiring Manager via Teams, followed by a panel interview and reference checks. Communication is handled via Workable—check your spam folder for emails from *@outbound.workable.com.
We do not accept unsolicited applications from agencies or recruiters.
Debiopharm is an independent biopharmaceutical company based in Switzerland with headquarters in Lausanne(VD) and a manufacturing site in Martigny (VS).We are committed to developing innovative therapies that target high unmet medical needs in oncology and infectious diseases with a broad range of expertise in drug development, drug manufacturing as well as investment in start-ups. Through our unique business model, we identify high-potential compounds and technologies for in-licensing, clinically demonstrate their safety and efficacy and then select large pharmaceutical commercialization partners to maximize patient access globally.
Debiopharm is an independent biopharmaceutical company based in Switzerland with headquarters in Lausanne(VD) and a manufacturing site in Martigny (VS).
We are committed to developing innovative therapies that target high unmet medical needs in oncology and infectious diseases with a broad range of expertise in drug development, drug manufacturing as well as investment in start-ups.
Through our unique business model, we identify high-potential compounds and technologies for in-licensing, clinically demonstrate their safety and efficacy and then select large pharmaceutical commercialization partners to maximize patient access globally.
