Analytical Development Technician

Empleado permanente, Tiempo completo · Noain - Jornada Turnos y Festivos

Tus tareas
  • The successful candidate will join 3P Biopharmaceuticals, in Navarra Spain, as a Technician (Senior Scientist) of the Analytical Development Department.
  • The candidate will be expected to be key member of the Analytical Development group and will have responsibilities within the physiochemical and protein characterization teams, with activities to develop and qualify and run physiochemical and protein characterization methods.
  • The candidate will be expected to provide development oversight, know-how and technical input into specific tasks and into the group in general, in addition to the testing, documentation and review of activities for the development and qualification of methods, testing and review of development materials, and contribution to routine laboratory activities.
  • Proficiency and capability in managing multiple projects in a fast paced environment with client interaction is expected.

Tu perfil
Assessment criteria:

  • At least three years experience in either Quality Control or Analytical Development groups from a related industry, with a preference from within the biopharmaceutical industry.
  • Profound experience in the physiochemical analysis of biomolecules by HPLC and related techniques, along with various detection technologies and softwares.
  • Experience with Mass Spec analysis of biomolecules, particularly proteins using Q-ToF will be mandatory. In particular the characterization of molecules such a monoclonal antibodies for mass, amino acid sequence, PTMs and glycans and/or other attributes would be advantageous.
  • Experience in the development on non-compendial methods for analysis of biomolecules within a regulated environment
  • Experience in the validation of such methods would also be highly valued.
  • Experience in the preparation and review of documentation (SOPs, Development Reports, Validation Reports, protocol) in English to regulatory standards is essential.
  • Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment.
  • Capable to identify technical and scientific problems and propose solutions.
  • Experience in performing stability, formulation and characterization studies of biomolecules is beneficial.
  • Proficiency to work within regulatory guidelines.
¿Por qué nosotros?
  • Immediate incorporation in a young and motivated working environment, in a company in full expansion.
  • Attractive remuneration according to experience.
Quiénes somos
3P Biopharmaceuticals es una compañía biotecnológica CDMO (Contract Development Manufacturing Organization) especializada en el desarrollo de procesos y fabricación GMP de medicamentos biológicos y productos de terapia celular.

Gracias a su equipo altamente cualificado, 3P apoya a sus clientes ofreciendo soluciones en todas las etapas de desarrollo del biofármaco: desde las fases iniciales de investigación, preclínicas y clínicas hasta fases comerciales.


Su larga experiencia en proyectos que abarcan todas las etapas de desarrollo y fabricación en tres diferentes sistemas de expresión (células de mamífero, bacterias y levaduras), su flexibilidad y adaptación junto con su tecnología de última generación y su gran capital humano, la han convertido en referente para el mercado biotech europeo y de Estados Unidos.


Estamos ansiosos por conocerte!
Gracias por plantearte una carrera en 3P Biopharmaceuticals. Por favor, rellena el siguiente formulario. Si tienes problemas al subir documentos, envíalos por correo electrónico a recruitment@3pbio.com.

Por favor, sube tu currículum y una breve carta de motivación.

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