IT Quality Applications Specialist

Neotalent Conclusion is one of the leading Iberian specialists providing services in Information Technology and Engineering services. As part of the Netherlands-based organization Conclusion, which has an ecosystem of over 25 companies and 3,600 employees, we are focused on increasing the technological capacity of our clients and the digital transformation of their application ecosystems. We are talent specialists, attracting the best people and combining them with the needs of the most ambitious projects, at the right time. Our success comes from our investments in innovation, our focus on results, and, above all, the guarantee that our people will have happy and rewarding careers. With over 25 years of solid experience, Neotalent Conclusion has established its presence in key locations, including Lisbon, Porto, and Madrid. The company currently has more than 950 professionals in the different areas in which it operates. Neotalent, the responsive people. Find out more

about us
at www.neotalentconclusion.com. Role Overview We are looking for an IT Quality Applications Specialist to integrate our teams in a project within a highly regulated international environment. In this role, you will support and enhance Quality, Regulatory and Laboratory Systems (QRLS), ensuring application reliability, compliance, and continuous improvement across business-critical platforms. You will work closely with business users, quality teams, technical stakeholders, and external vendors, contributing to application support, system validation, documentation, and implementation initiatives. What you will do
- Provide functional and technical support for quality, regulatory, and laboratory applications, investigating and resolving incidents;
- Monitor system availability and performance, identifying improvement opportunities and ensuring reliable operations;
- Troubleshoot interfaces between applications and laboratory equipment, analysing root causes and coordinating resolutions;
- Collaborate with business, quality, development, and vendor teams to support system enhancements and operational needs;
- Coordinate application implementations and rollout activities, ensuring proper documentation, compliance, and stakeholder communication;
- Manage user access requests and system security activities in accordance with internal procedures;
- Produce and maintain system lifecycle documentation, including URS, Functional Specifications, Design Specifications, and validation deliverables;
- Ensure compliance with GxP requirements, quality procedures, and documentation standards. What you are like
- Proficient in IT application support within enterprise environments;
- Experienced with Quality Management Systems (QMS) and Document Management Systems (DMS);
- Familiar with regulated industries, ideally pharmaceutical, life sciences, food, or similar sectors;
- Strong knowledge of Computer System Validation (CSV) principles and documentation practices;
- Skilled in troubleshooting application issues and integrations involving laboratory systems and equipment;
- Proficient in technical documentation writing and communication in English;
- Comfortable working with cross-functional teams, business stakeholders, and third-party vendors;
- Experienced in application implementation projects and rollout activities;
- Knowledge of solutions such as Veeva, Empower, LabWare, or equivalent platforms is a plus;
- Familiar with Microsoft Office tools and able to quickly adapt to new technologies and applications.
- Work on challenging projects for big clients;
- Learn more about emerging technologies;
- Possibility of working remotely;
- Design your career plan;
- Access to continuous training and certifications;
- Evolve through our internal mobility program;