- 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.
- Effectively convey scientific insights, experimental plans, and results to internal teams, external clients and conferences, serving as internal technical subject matter expert.
- 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.
- 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.
- 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.
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Process and Analytical Scientist – Cell&Gene Therapy - Vimodrone, Italia - Eurofins
Descrizione
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.
The preferred candidate should display a keen attention to detail, self-driven motivation, and proficiency in hands-on laboratory tasks. Essential qualifications include adept lab management and organization skills, as well as prior exposure to operating and maintaining bioreactors and downstream equipment, preferably backed by a proven experience in the production of cell therapies and/or viral vectors for pre-clinical and clinical settings.
Main responsibilities are:
Above all, the ideal candidate embodies curiosity and engagement, proactively seeking to propel the scientific and technical advancement of our new CDMO division.
Qualifications
Additional Information
What is our offer:
Interested in this challenging job?
Please send your application including CV and motivation letter, including authorization in using personal data.
