• Background: Degree related to research in biomedicine (Science, Biology, Biochemistry, Chemistry, Pharmacy ...) or related engineering.

  • Higher degree related.

  • Ability to propose potential process improvements and essays. Results analyses.

  • Previous experience in GMP manufacturing and/or bioprocesses.

  • Spoken and written communication skills (both in Spanish and English).

  • Team working skills and ability to work under deadlines.


Job duties (summary)

  • Execute Lentiviral vectors manufacturing processes according to GMP manufacturing guides.

  • Drafting of manufacturing protocols, standardized operating procedures (SOPs) and other relevant manufacturing guides.

  • Comply with and ensure compliance with internal manufacturing standards.

  • Be part of a multidisciplinary team to carry out process optimizations and researches.

  • Carry out maintenance of manufacturing areas to guarantee their status and compliance with GMP regulations.


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Contact us

Mikeletegi Pasealekua 81, San Sebastián 20009, Gipuzkoa (SPAIN)