KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, 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 it 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 200 employees, and it is committed to promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion. We are looking for an analyst for our Department of BIO QC where we analyze mainly biological drugs (proteins, peptides, polysaccharides, etc.). Responsibilities Perform quality control tests by HPLC methods. Perform the work in an environment of compliance with Good Manufacturing Practices. Why should you work with us? You will be part of an experienced and dynamic team in a growing Contract Research Organization. We encourage challenges and autonomy, so you will have opportunities to learn and grow. Social benefits platform available for employees. Flexibility in check-in and check-out times. Our headquarters are located in a privileged location at the foot of Collserola Park, the green lung of Barcelona. Requirements Person with teamwork skills. Experience with analytical techniques such as: HPLC, ELISA, etc. Higher Degree Training of Analysis and Quality Control Laboratory. Experience working in GMP and GLP environments will be valued. 2 years of experience in similar functions in the pharmaceutical industry. Sector: Pharmaceutical and biopharmaceutical#J-18808-Ljbffr