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A rapidly growing Contract Research Organization is seeking an analyst for its Microbiology Department. The role includes performing microbiological analyses and ensuring the safety and quality of products. Candidates should have relevant vocational training and at least 1 year of experience in the pharmaceutical industry. Strong problem-solving skills and teamwork ability are essential. Knowledge of endotoxin testing and GMP environments is preferred.
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 in 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 in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.We are looking for analysts for our Microbiology Department, where critical activities are carried out to ensure the microbiological safety and quality of products and processes.Main responsibilities include :
Microbiological analysis of raw materials and finished products (TAMC, TYMC, pathogen testing, sterility tests, among others).Water sampling and analysis.Endotoxin testing (Gel Clot method, kinetic chromogenic, and turbidimetric methods).Microbial growth testing in culture media.Sample preparation and support for microbiological analytical techniques.Testing of culture media.Working in an environment regulated by GMP standards.Requirements :
Higher Vocational Training in Laboratory Analysis and Quality Control or a related field.Minimum of 1 year of experience in similar roles within the pharmaceutical industry.Knowledge of endotoxin testing.Intermediate level of English.Experience in GMP environments is a plus.Ability to work as part of a team.A proactive person with strong problem-solving skills.
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