Técnic@ de Producción USP

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

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Your mission
The successful candidate will join 3P Biopharmaceuticals, in Navarra, Spain, as an upstream manufacturing technician in Industrial Scale up and Manufacturing Department.
The candidate will be expected to provide development oversight, know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the upstream manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as, contribution to routine laboratory activities.

Proficiency and capability in managing multiple projects in a fast paced environment with client interaction is expected.
Responsibilities will include (but not limited to):

•    Creation of operating procedures & other relevant documentation for large scale manufacturing.
•    Execution of commercial manufacturing processes according to established work instructions.
•    Adheres to Good Manufacturing Practices and Standard Operating Procedures.
•    Takes part in investigations and optimizations of processes using scientific, engineering and lean principles.
•    Operates all USP production equipment within the assigned functional area.
•    Assists with reviewing batch and manufacturing reports in conjunction with Quality representative and provide input to related investigations and QA audit activities. Engages in and supports culture of continuous 
improvem ent and operational excellence through ownership of improvement for work processes, equipment and safe work environment.


Your profile
•    From two to three years experience in either R&D or manufacturing departments in upstream processes, within the biopharmaceutical industry or the academic field.
•    Knowledge of microbiology and/or cell culture is a must.
•    Knowledge of biochemistry and metabolic pathways is essential.
•    Experience in working with bioreactor and filtration systems is desirable.
•    Experience in working on upstream processes with yeast, bacterial and mammalian cells would also be highly valued.
•    Experience in GMP environment is an advantage.
•    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 managing studies and/or small-teams are expected.
•    Proficient verbal and written communicator.
•    Proficiency to work within regulatory guidelines.

Why us?
  • Attractive remunaration according to the proven 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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