Analyst (Biological Quality Control)

Location: Cerdanyola del Vallès (Spain)
Contract: Permanent
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), 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.

Job description

Buscamos a un/a analista para nuestro Departamento de BIO QC donde se analizan principalmente fármacos biológicos (proteínas, péptidos, polisacáridos, etc.).

Las responsabilidades del puesto son:

Realizar control de calidad de productos biológicos (proteínas, vacunas...) con técnicas HPLC
Realizar el trabajo en un entorno de cumplimiento de Buenas Prácticas de Fabricación (GMP).

We are looking for an analyst for our Department of BIO QC where we analyze mainly biological drugs (proteins, peptides, polysaccharides, etc.).

The responsibilities of the position are:

Perform quality control tests by HPLC methods
Perform the work in an environment of compliance with Good Manufacturing Practices

¿Por qué deberías trabajar con nosotros?

Serás parte de un equipo experimentado y dinámico en una Organización de Investigación por Contrato en crecimiento.
Fomentamos los desafíos y la autonomía, por lo que tendrás oportunidades de aprender y crecer.
Empresa con conciencia de género.
Plataforma de beneficios sociales disponible para los empleados.
Flexibilidad en las horas de entrada y salida
Nuestra sede se encuentra en un lugar privilegiado a los pies del Parque de Collserola, el pulmón verde de Barcelona.

Why should you work with us?

You will be part of an experienced and dynamic team in a growing Contract Research Organization.
We encourage challenges and autonomy, so you will have opportunities to learn and grow.
Gender conscious company.

Social benefits platform available for employees.
Flexibility in check-in and check-out times.
Our headquarters are located in a privileged location at the foot of Collserola Park, the green lung of Barcelona

Requirements

REQUISITOS:

Persona con aptitudes para trabajar en equipo.
Experiencia con técnicas analíticas como: HPLC, ELISA, ...
Formación de Grado Superior de Laboratorio de Análisis y Control de Calidad.
Inglés nivel medio
Se valorará la experiencia trabajando en entornos GMP y GLP.
Experiencia de 2 años en funciones similares en la industria farmacéutica.

REQUIREMENTS:

Person with teamwork skills.
Experience with analytical techniques such as: HPLC, ELISA, …
Higher Degree Training of Analysis and Quality Control Laboratory.
English medium level.
Experience working in GMP and GLP environments will be valued.
2-years experience in similar functions in the pharmaceutical industry. ).

Job closed

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

Check our other jobs