Process and Analytical Scientist

2 settimane fa

Vimodrone, Italia Eurofins Italy BioPharma Product Testing A tempo pieno

**Company Description**
Con 900 laboratori, circa 61.000 dipendenti, oltre 200.000 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 non-viral 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 problem-solving 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 fast-paced 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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