We are a specialty vaccine company that develops, manufactures, and commercializes prophylactic vaccines for infectious diseases addressing unmet medical needs. We take a highly specialized and targeted approach, applying our deep expertise across multiple vaccine modalities, focused on providing either first-, best- or only-in-class vaccine solutions.

Responsibilities

As Senior DevOps Engineer, you will play a pivotal role in ensuring the quality and reliability of our cloud ERP system (including validation activities). You will be responsible for developing, implementing, validating, and maintaining robust quality assurance processes and procedures to guarantee the functionality, performance, and usability of our ERP solutions. Working closely with cross-functional teams on a global level, you will identify areas for improvement, drive quality initiatives, and champion best practices throughout the development lifecycle.

Your main tasks includes:

• Develop, implement, and maintain automated testing tools for ERP and Cloud systems to enhance testing efficiency.
• Design and manage CI/CD pipelines using Azure DevOps.
• Create and execute test cases, scripts, and validation protocols (IQ/OQ/PQ) for system functionality, performance, and compliance.
• Analyze test results, track and resolve defects, and collaborate with cross-functional teams to ensure quality outcomes.
• Develop and document validation strategies aligned with regulatory standards (FDA, GxP, GAMP) and company policies.
• Review and approve validation documentation, ensuring accuracy and regulatory compliance.
• Stay current with industry trends, support audits, and contribute to continuous improvement of ERP QA processes.
  
  
  

• Bachelor's degree in Computer Science, IT, or related field

• Minimum 3 years of experience in IT systems engineering
• Strong knowledge of ERP systems and experience with testing tools and methodologies (SAP, Microsoft Dynamics, Azure DevOps, API testing, CI/CD, Jira, Confluence)
• Proficiency with automated testing frameworks (e.g. Selenium, RSAT)
• Experience in pharmaceutical industry is an asset (validation principles, regulatory standards)
• Excellent analytical, documentation, and troubleshooting skills with high attention to detail
• Excellent verbal and written communication skills in English
  
  
  

Working with Valneva means being part of a global biotech company with a clear vision to make a meaningful impact in the world. At Valneva, you can expect a dynamic and innovative work environment characterized by an open, appreciative company culture and exciting, impactful assignments. Enjoy the benefits of flat hierarchies, an international atmosphere, and regular company events that foster collaboration and connection.

Additionally, we offer:

• Work Life Balance: Flexitime & Compensation days
• Financial perks: Performance-related bonus & Lunch vouchers
• Lifelong learning: Unlimited access to LinkedIn Learning
• Health & Wellbeing: Free access to sports and fitness activities via myClubs & Office Massages

Join us and shape the future of biotechnology! Please send your CV in English!

Due to legal reasons we are obliged to disclose the minimum salary for this position, which is € 60.000 gross per year based on full-time employment. However our salaries are market oriented and in line with your qualifications and experience.