ANALISTA QUIMICO /CHEMISTRY ANALYST (STABILITY)

Location: Cerdanyola del Vallès (Spain)
Contract: Contract for Works and Services
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality

Kymos

We are an innovative and fast-growing CRO offering you the opportunity to develop your career in an excellent working environment. Kymos Group is a scientific-technical services company directed to companies of the chemical-pharmaceutical and veterinary sector.

KYMOS offers a wide range of analytical services in Medicinal Chemistry to optimize the research, the development and the quality control for innovative, generic and biological drug substances and drug products from the preclinical stage to market.

KYMOS also has an extensive experience in developing and validating bioanalytical methods and sample analysis in any biological matrix using the latest technology. Mass spectrometry and immunology laboratories are available to carry out small molecule and biologic projects.

KYMOS is also an international group, Kymos Group, with sites in Italy, PHARMAPROGRESS and in Germany, PROLYTIC.

Job description

Buscamos a analistas para nuestro departamento de Análisis Químico y Control de Calidad donde se analizan principalmente materias primas y especialidades farmacéuticas.

Las responsabilidades son:

Dar soporte a los químicos analíticos en la preparación de muestras y en el uso de diversas técnicas analíticas (potenciometrías, Karl Fisher, Cromatografia Líquida de Alta Resolución (HPLC), cromatografía de gases, UV, Test de disolución, etc)
Realizar el trabajo en un entorno de cumplimiento de Buenas Prácticas de Laboratorio y GMP

We are looking for analysts for our Department of Chemical Analysis and Quality Control where we analyze mainly raw materials and pharmaceutical specialties.

The responsibilities of the position are:

Support analytical chemists in the preparation of samples and the use of various analytical techniques (potentiometries, Karl Fisher, high performance liquid chromatography (HPLC), gas chromatography, UV, dissolution test, etc)
Perform the work in an environment of compliance with Good Laboratory Practices and GMP.

Requirements

Persona con aptitudes para trabajar en equipo
Formación de Grado Superior de Laboratorio de Análisis y Control de Calidad.
Inglés nivel medio
Se valorará la experiencia en trabjar en entornos GXP y en departamento de control de calidad
Experiencia de 1 año en funciones similares en la industria farmacéutica

Person with teamwork skills
Higher Education Laboratory of Analysis and Quality Control.
Medium command of English
Experience in working in GXP environments and in a quality control department
1 year experience in similar roles in the pharmaceutical industry

Job closed

Location: Cerdanyola del Vallès (Spain)
Contract: Contract for Works and Services
Working day: Full time
Sector: Pharmaceutical and biopharmaceutical
Vacancies: 1
Discipline: Quality

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