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 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.
Position Overview
We are looking for analysts for our Quality Control Department, where we analyze mainly raw materials, finished products, and pharmaceutical specialties.
Responsibilities
Requirements
Benefits
KYMOS GROUP 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.
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