Quality Control Scientisten Barcelona.

¿ Tienes experiencia realizando análisis físico- químicos ?? ¿ Dominas el HPLC ? ¿ Quieres evolucionar a una posición de Scientist o Técnico ?

our client

Kymos Group es una organización de investigación por contrato (CRO) de origen español y presencia internacional.
Está especializada en ofrecer servicios científico-técnicos, bioanalíticos y de control de calidad (CMC).
Su actividad da soporte a las industrias farmacéutica, biotecnológica, veterinaria y cosmética en sus fases de desarrollo.
Ayuda a optimizar los tiempos de comercialización mediante laboratorios certificados bajo normativas GMP y GLP.

your functions

Kymos is hiring a Scientist in Chemical Analysis for our Quality Control department:

Position Description:

We offer a position in the Pharmaceutical Chemical Analysis Department as a Scientist responsible for the analysis of active ingredients and pharmaceutical specialties.
The role involves designing, supervising, and conducting studies on the development and validation of analytical methods for drug control, stability studies, quality control, etc. Analytical techniques employed include HPLC, GC, potentiometry, Karl Fisher, UV, dissolution testing, etc.
Draft, review, and manage technical documentation associated with the studies (protocols, reports, standard procedures, certificates of analysis, etc.)
Supervise and mentor laboratory analysts and technical staff during experimental work, promoting scientific excellence and GMP compliance.

position requisites

• Formación

  : Licenciado

• Idiomas

  : Inglés: B2

• Conocimientos

  : análisis hplc

• Experiencia

  : 1 año

We are seeking an individual with a Bachelor's degree in Chemical Sciences (Analytical Orientation). A Master degree is highly valued.
The ideal candidate has some knowledge in HPLC, GC techniques, and have a basic understanding of an analytical development department.
Some experience in the development and validation of new analytical methods for quality control of pharmaceuticals is valued.
Previous experience in chemical analysis of active ingredients and pharmaceutical formulations in a Quality Control or Analytical Development department of a pharmaceutical or related company is preferred.
Experience working with GLP and GMP is required.
Minimum English language proficiency level: First Certificate.

your benefits

Working in a dynamic company with a highly qualified growing team
Professional development and collaborative environment and a culture of empowerment.
Flexible 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.

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