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 Liason 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.
Tareas
We are hiring a Quality Scientist for our Biologics Quality Control Department. The Scientist will be responsible for the following functions:
Tasks
* Review and audit the department's primary data.
* Collaborate in the internal improvement of data recording processes.
* Collaboration in the GMP investigations of the department (Deviations, OOS, CAPA,...)
* Collaboration in the monitoring and analysis of the department's KPI's.
* Elaboration of SOP's and analysis guides of the Department.
* General administrative tasks (purchase management, laboratory management, documentation archiving,...)
Education/Skills
* Degree in health sciences or similar
* Experience in GMP environment, with specific knowledge of pharmaceutical analytical techniques
* Interest in quality management
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