Técnico Validación de Sistemas Informatizados | Pharma (Madrid)

Técnico Validación de Sistemas Informatizados | Pharma (Madrid)

29 ago
|
Kymos Group
|
Madrid

29 ago

Kymos Group

Madrid

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), Germany (Frankfurt), Denmark (Copenhagen) 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 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 330 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.
Kymos Group ,



we provide specialized analytical services to the pharmaceutical industry in regulated GMP and GLP environments. Our laboratories are equipped with a wide range of analytical instruments and computerized systems, including solutions such as LIMS, Empower, laboratory software, and other corporate systems . We are currently looking for someone to join our Computer System Validation — CSV area, based in Cerdanyola del Vallès, Barcelona . We are looking for a profile with some previous experience or knowledge in CSV, quality, laboratory environments, or computerized systems, who is willing to continue developing in a regulated and highly technical environment.
Main objective

To support the validation, maintenance, and review activities of computerized systems used in the laboratory and in other company processes, ensuring compliance with applicable regulatory requirements in GxP environments.
Main responsibilities

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📌 Técnico Validación de Sistemas Informatizados | Pharma (Madrid)
🏢 Kymos Group
📍 Madrid

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