• Location: Cerdanyola del Vallès (Spain)
• Contract: Fixed-term
• Working day: Full time
• Sector: Pharmaceutical and biopharmaceutical
• Vacancies: 1
• Discipline: R&D
• Work modality: On site
  
  

Kymos Group

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), and Germany (Frankfurt) and a Liasson 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 250 employees, and it is committed in promoting diversity, gender-equality, well-being, and initiative within its members, encouraging career development and internal promotion.

Job Description

Buscamos a un analista para nuestro Departamento de Inmunología. para cubrir una baja temporal.

Las Responsabilidades Del Puesto Son

• Realizar análisis de fármacos biológicos y anticuerpos (proteínas, péptidos, etc.) en matrices biológicas (plasma, suero, etc.) de muestras procedentes de estudios clínicos y preclínicos.
• Realizar el trabajo en un entorno de cumplimiento de Buenas Prácticas de Laboratorio (BLP/GLP).
  
  

We are looking for an analyst for our Immunology Department to cover a temporary leave.

The Responsibilities Of The Position Are

• Perform the analysis of biological drugs and antibodies (proteins, peptides,...) in biological matrices (plasma, serum,...) of samples from clinical and preclinical studies.
• Perform the work in an environment of compliance with Good Laboratory Practices (GLP).
  
  

Requirements

• Formación profesional de Grado Superior Sanidad Especialidad Laboratorio Clínico.
• Experiencia en métodos inmunológicos RIA, ELISA, ECLA.
• La experiencia en ensayos celulares será una ventaja.
• Inglés nivel medio.
• Se valorará la experiencia en trabajar en entornos GLP.
• Capacidad de trabajar en equipo.
• Higher Education Laboratory of Clinical laboratory.
• Experience in immunological methods such as RIA, ELISA, ECLA.
• Experience in cell assays will be a plus.
• Good command of English.
• Experience in working in GLP environments.
• Good team player.
  
  

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• Location: Cerdanyola del Vallès (Spain)
• Contract: Fixed-term
• Working day: Full time
• Sector: Pharmaceutical and biopharmaceutical
• Vacancies: 1
• Discipline: R&D
• Work modality: On site
  
  

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