Scientific Product Development Manager
20 ore fa
About Eurofins Italy Biopharma Product Testing
">With over 900 laboratories, approximately 61,000 employees, more than 200,000 analytical methods, a presence in 54 countries, and an annual revenue of 6.7 billion EUR, Eurofins Scientific is a global leader in third-party laboratory services for the Pharmaceutical, Food, Environmental, and Consumer Products sectors.
">We are committed to strengthening our BioPharma division to provide value to clients worldwide. We are seeking highly motivated and result-oriented individuals who wish to join our solid and dynamic organization.
">The Scientific Product Development Manager will be responsible for hands-on activities to establish Analytical and Manufacturing processes for the new C&G CDMO division, as well as related services for clients.
">S/he will provide expertise to support C&G activities, working closely with cross-functional teams, and play a key role by setting the right process and quality to address company and client needs.
">Main Responsibilities:
">">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 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 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.">">Requirements:
">">MS (or equivalent experience) in pharmaceutical sciences, medical biotechnology, biology, or a 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 considered 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, communicate appropriately, initiate problem-solving processes, and propose remedial actions.">Excellent oral communication, reporting, and presentation skills.">Good English skill is preferable.">">What We 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 of €80,000 - €110,000 per year, depending on experience, based on market practice + ticket restaurant and company welfare.">About Our Team:
">We are a dynamic team that values innovation, collaboration, and continuous learning. If you are a motivated and results-driven individual who is passionate about Cell&Gene Therapy, we encourage you to apply for this exciting opportunity.
">"EUR 80,000-EUR 110,000", A Competitive Salary Package, including benefits like ticket restaurant and company welfare, reflects the importance we place on attracting and retaining top talent.
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