Overview KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain (Cerdanyola del Vallés- Barcelona), Italy (Monsano-Ancona), and Germany (Frankfurt) and a Liaison office in South Korea (Seoul), offering comprehensive bioanalytical and CMC analytical services to the life sciences industry. Its laboratories are GMP and GLP certified and GCP compliant, and have been successfully inspected by EMA, FDA, and ANVISA. KYMOS GROUP is devoted to providing high quality and added value services to its partners and is highly oriented to innovation, offering services of research, development and quality control in many different fields such as small molecules, proteins, antibodies, nucleic acids, and advanced therapies. KYMOS GROUP has a young and dynamic staff of more than 250 employees, and is committed to promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion. Key responsibilities Provide timely support to users by handling incidents and inquiries through the designated tools (e.g., ServiceDesk Engine), ensuring effective resolutions or workarounds to minimize business impact. Develop, configure, and validate subroutines to meet required functionalities, including preparing all relevant documentation (user manuals, validation plans, functional specifications, etc.). Collaborate with external consultants and the IT department to ensure optimal system performance. Proactively identify areas for improvement and contribute to driving the LIMS system towards higher performance, increasing overall company efficiency. What we offer A permanent contract and a competitive salary based on experience and expertise. Flexible work schedule with some level of remote working. The opportunity to join a young, multicultural, and dynamic team in a fast-growing company with international exposure. An environment that encourages autonomy and challenges, offering plenty of opportunities for learning and professional growth. Requirements Strong desire to learn and develop expertise in LIMS software and laboratory data management processes. Flexible, committed, and an excellent team player. Strong problem-solving skills, with the ability to listen, understand user needs, structure and analyze requirements, and propose effective solutions. Advanced English level (C1); Spanish is a plus. Valuable Qualifications Prior LIMS user experience (LabWare LIMS preferred) or experience with other ERP systems. Experience working in a pharmaceutical laboratory environment (Quality Control, Analytical Development, etc.). Previous exposure to software tools or programming in a laboratory setting. Strong analytical and problem-solving abilities. Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic. Sector : Pharmaceutical and biopharmaceutical J-18808-Ljbffr