Scientist to join our Biologics and Advanced Therapies Quality Control External Recibidos Resumir este correoen Barcelona.

detalle oferta

  • tipo de contrato Indefinido

  • jornada Completa

  • modalidad Presencial

  • sector Life Science

  • salario

    30.000-40.000 €/año
  • puesto

    medical scientist
  • nº vacantes

    1
  • localidad

    Barcelona
  • provincia

    Barcelona
  • especialidad

    Química Farma
  • subespecialidad

    Química Farma
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Amplía la información sobre el proceso contactando con:

Alicia Olaya Garcia

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our client

KYMOS es una organización de investigación y laboratorio por contrato (CRO/CLO) de origen español que presta servicios científicos a nivel global para los sectores farmacéutico, biotecnológico, veterinaria y cosmética.

¿Qué hace?: Ofrece soporte integral en bioanálisis y control de calidad (CMC), abarcando desde las fases iniciales de I+D y ensayos clínicos hasta la liberación de lotes comerciales.

Especialidad: Trabaja tanto con moléculas pequeñas (genéricos) como con productos biológicos complejos y terapias avanzadas.

Presencia y Calidad: Tiene su sede en Barcelona, filiales en Italia, Alemania y Dinamarca, y cuenta con certificaciones internacionales clave (GMP / GLP) avaladas por agencias como la FDA y la EMA.

your functions


We are seeking a highly motivated Scientist to join our Biologics and Advanced Therapies Quality Control team. This role, reporting to the Department Manager, focuses on the analysis of biological products in a GMP-regulated environment.
Key responsibilities:
Design, execution, and oversee of analytical method development and validation studies for biologic products, including monoclonal antibodies, recombinant proteins, and advanced therapies.
Hands-on experience with techniques such as HPLC, capillary electrophoresis, ELISA, protein quantification (e.g., BCA, UV), and other relevant biochemical methods.
Lead and manage assigned development and validation projects, ensuring timely execution, compliance with regulatory requirements, and effective communication with internal and external stakeholders.
Draft, review, and manage technical documentation including method validation protocols and reports, SOPs, risk assessments, and technical justifications.
Collaborate with cross-functional teams including Quality Assurance and Marketing to support method development and validation.
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

Bachelor's or higher degree in Biochemistry, Biotechnology, Pharmacy, or a related life science field.
Solid hands-on experience in analytical method development and validation for biologics, particularly using HPLC, capillary electrophoresis, and immunoassay-based techniques.
In-depth understanding of GMP requirements and ICH guidelines relevant to analytical method validation.
Experience with HPLC and Capillary electrophoresis development will be considered a strong asset.
Excellent organizational and documentation skills, with the ability to manage multiple projects simultaneously.
English level equivalent to Cambridge First Certificate (B2) or higher.
Willingness and availability to work the afternoon shift (2:00 PM ¿ 10:00 PM).

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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