Tus tareas

• To be a member of the manufacturing team and contribute within the DNA synthesis and purification process applied to manufacturing, process development, tech transfers and process validation.
• Support to the technicians of the area.
• To be involved in the manufacturing process to obtain synthetic DNA with the specifications required by clients.
• Contribution to routine laboratory activities.
• Writing SOPs.
• Primary data record.
• Verification of laboratory equipment and instruments.
• Execute the design, construction, and development of DNA molecules for client’s projects.
• Collaborate with generation of the documentation associated to the development project.
• Participate in R&D projects.
• Train staff on specific techniques and support the team with technical knowledge.
• Collaborate in the maintenance of the TAAV quality system.

Tu perfil

• Bachelor level education (Biochemistry /Biotechnology/Molecular Biology or equivalent degree) or experience in industry and/or academia.
• Applicants must have knowledge and hands-on experience.
• Good IT skills including the use of software like SnapGene, good knowledge of Microsoft Office…
• Ability to follow SOPs and to complete documentation (lab books, forms, logbooks, process instructions).
• Time efficiency and ability to work independently. Excellent problem-solving skills.
• Good communication skills both verbal and written.
• Proactive and available to organize their own work with continuous improvement mind set.
• Reliable, enthusiastic, and self-motivated.

¿Por qué nosotros?

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¿Quiénes somos?

Our Goal is to provide the gold-standard DNA for AAV manufacture

TAAV started as a Joint Venture formed by two leading biotechnology organizations within synthetic DNA and AAV manufacturing.

In 2020 TAAV launched its state-of-the-art facility located in San Sebastian, Spain. The facility is comprised of four suites and additional support labs, that are specifically designed for the manufacture of high quality neDNA™.

TAAV Biomanufacturing Solutions, S.L.U. (TAAV) is a contract development and manufacturing organization (CDMO) owned by Asklepios Biopharmaceutical, Inc. (AskBio) a gene therapy company wholly owned and independently operated as a subsidiary of Bayer AG. Our proprietary in vitro DNA amplification technology leads the way in the production of high-quality enzymatic DNA (neDNA™) as an alternative to plasmid DNA that aims to enable better rAAV production.

We view neDNA™ as a disruptive technology in the DNA market creating a new industry standard for transfection-based AAV production. Our synthetic process leads to high yield at small scales, shortening manufacturing timelines, facilitating quicker production of AAV and increasing safety by eliminating residual bacterial sequences of plasmid DNA in the AAV product.

Discover our TAAV-produced dbDNA™ process for rAAV manufacturing.