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.

Descripción de la oferta

Buscamos a analistas para nuestro departamento de Analytical Development & Validation.

Las principales responsabilidades son:

- Dar soporte en experimental.
- Análisis de materias primas y productos acabados.
- Dar soporte a los análisis en la preparación de muestras y en el uso de diversas técnicas analíticas.
- Realizar el trabajo en un entorno de cumplimiento de GLP y GMP.

We are looking for analyst for our Analytical Development & Validation Department.

Main responsibilities are:

- Experimental support.
- Analysis of raw materials and finished products.
- Support analysis in sample preparation and the use of various analytical techniques.
- Perform work in a GLP and GMP compliance environment.

Requisitos

Requisitos:





- Persona con aptitudes para trabajar en equipo.
- Experiencia con proyectos de potenciometría.
- Experiencia con técnicas analíticas como: HPLC, Cromatografía de Gases, etc.
- Formación de Grado Superior de Laboratorio de Análisis y Control de Calidad.
- Inglés nivel medio.
- Español avanzado.
- Se valorará la experiencia trabajando en entornos GMP y GLP.
- Experiencia de 1 año en funciones similares en la industria farmacéutica.

Requirements:

- Person with teamwork skills.
- Experience with potentiometry projects.
- Experience with analytical techniques such as: HPLC, Gas Chromatography, etc.
- Higher Degree Training of Analysis and Quality Control Laboratory.
- English medium level.
- Spanish proficiency level.
- Experience working in GMP and GLP environments will be valued.
- 1-year experience in similar functions in the pharmaceutical industry.

If you join us, you will enjoy:
- Working in a dynamic company with a highly qualified growing team
- Professional development and collaborative environment and a culture of empowerment.
- Versátil Working Hours and intensive schedule on Friday.
- Hybrid work, but mainly in the office.
- Access to the employee benefits flexibility platform.
- 23 vacation days per year plus 24th and 31th of December.
- Fully stocked canteen and rooftop space (coffee, fruits, snacks, and beverages).
- Our headquarters located in Cerdanyola del Vallés, an amazing place at the foothill of Collserola Park, the green lung of Barcelona, with our Rooftop terrace.

Kymos considers diversity and inclusion as key development priorities, with one of our main goals being to promote a culture that embraces differences and celebrates unique talents. For this reason, we are committed to equal opportunities for all people, regardless of gender, nationality, sexual orientation, gender identity, age, religion or any other personal characteristic.

📌 Development & Validation Analyst (Cerdanyola del Vallès)
🏢 Kymos
📍 Cerdanyola del Vallès