Upstream Bioprocess Technician – GMP & Scale-Up

3pbiovian

Noáin

In loco

EUR 28.000 - 42.000

Tempo pieno

14 giorni+
Generatore di candidature

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Vantaggi offerti da questo lavoro

Relocation assistance
41 days paid vacation
Flexible compensation plan
Learning & Development programs
Well-being initiatives

Descrizione del lavoro

3PBiovian is seeking an Upstream Technician to join the Manufacturing Operations team in Navarra. You will support scale-up, equipment entry, and process development for biologics produced in microorganisms.

The role emphasizes GMP adherence, training, and cross-department collaboration to ensure quality and timely delivery. Reporting to the USP Team Leader, you will help monitor quality indicators and participate in continuous improvement, with potential relocation support for non-local

Competenze

  • Bachelor's degree or higher in a related field with GMP/bioprocess exposure.
  • Experience with scale-up and manufacturing processes is valued.
  • Fluency in Spanish; English level B2+ is desirable.

Mansioni

  • Ensure timely planning of USP Scale-Up and Manufacturing activities.
  • Train personnel in charge and ensure proper capabilities.
  • Prepare and develop production processes for recombinant proteins/biologics in microorganisms.
  • Participate in audits and ensure GMP compliance within the team.
  • Record quality indicators and support investigations with the Team Leader.
  • Propose and implement process improvements and technology transfers.
  • Maintain documentation and oversee ERP-based order monitoring for USP production.

Conoscenze

GMP/GLP
Industrial-scale bioreactors
Cell cultures
Microbiological analysis
Upstream production
Biotechnology / Biopharma

Formazione

Bachelor's in Pharmacy
Biology
Biochemistry
Biotechnology
Chemistry
Chemical Engineering
IPPA

Strumenti

Office

Descrizione del lavoro

3PBiovian is seeking an Upstream Technician to join the Manufacturing Operations team in Navarra. You will support scale-up, equipment entry, and process development for biologics produced in microorganisms.

The role emphasizes GMP adherence, training, and cross-department collaboration to ensure quality and timely delivery. Reporting to the USP Team Leader, you will help monitor quality indicators and participate in continuous improvement, with potential relocation support for non-local

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