Process and Analytical Scientist

2 settimane fa

Vimodrone, Lombardia, Italia Eurofins Italy BioPharma Product Testing A tempo pieno

Company Description

Con 900 laboratori, circa dipendenti, oltre metodi analitici, una presenza diffusa in 54 paesi e un fatturato annuo di 6.7 BIL EUR, Eurofins Scientific è un gruppo internazionale leader nei servizi analitici conto terzi nei settori Farmaceutico, Alimentare, Ambientale e Consumer Products.


Eurofins nell'ottica di potenziare la sua divisione BioPharma, al fine di fornire valore a clienti di tutto il mondo, è alla continua ricerca di persone fortemente motivate e orientate al raggiungimento dei risultati che vogliano entrare a far parte di una realtà solida e dinamica.


Job Description Eurofins Biopharma Product Testing** is looking for a _Process and Analytical Scientist _that will be part of the CDMO team dedicated to Cell&Gene Therapy.

Function description:


The Process and Analytical Scientist will be accountable for hands-on activities to establish the Analytical and Manufacturing processes of the new C&G CDMO division, as well as for the performance of related services for clients.


She/He will provide expertise to support the C&G activities, working closely with cross-functional teams, and playing a relevant role by setting the right process and quality to address company and client's needs.


Main responsibilities are:

  • Support and execute Analytical and Manufacturing wet activities both in R&D and GMP classified spaces.
  • Work with the existing analytical team to integrate Cell and Gene capabilities.
  • Establish the manufacturing processes and analytical methods for cell therapies, such as viral and nonviral gene editing methods, production protocols for T and NK based therapies.
  • Establish the manufacturing processes and analytical methods for viral vectors, starting from the establishment of a LVV based platform (adherent and suspension protocols).
  • Support Tech Transfer.
  • Autonomously plan, execute, and analyze experiments.
  • Develop, draft and manage procedures, reports and key documentation as appropriate.
  • Collaborate with external providers and scientific partners to evolve, procure, and manage new equipment and processes.

Qualifications

  • MS (or equivalent experience) in pharmaceutical sciences, medical biotechnology, biology or related discipline. PhD or related degree is preferable.
  • Minimum of 3 years in Cell&Gene Therapy development and / or manufacturing experience in a GMP environment is preferable.
  • Experience in Viral Vector manufacturing is preferable.
  • Experience in downstream (chromatography, TFF) will be consider a plus.
  • Strong decision making and problemsolving skills.
  • International experience is considered a plus.
  • Excellent organization, facilitating and coordination skills. Ability to work independently as well as a member of a team in a dynamic and fastpaced environment.
  • Able to identify problematic situations, to communicate appropriately, to initiate problem solving processes and to propose remedial actions.
  • Excellent oral communication, reporting and presentation skills.
  • Good English skill is preferable.

Additional Information What is our offer**:

  • A position with responsibility within a dynamic company.
  • Working in an innovative and international environment together with a dynamic team.
  • Professional and personal development is supported.
  • Sustainable and meaningful approach in everything we do.
  • A salary, depending on your experience, based on market practice + ticket restaurant and company welfare.
**Interested in this challenging job?

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