Senior Scientist, DSP Process Engineer - Vitry-sur-Seine - Sanofi US

    Sanofi US
    Sanofi US Vitry-sur-Seine

    il y a 3 jours

    Description

    Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l'international, l'anglais étant la langue de travail.

    This job offer is accessible to all, regardless of gender.

    Job title: Senior Scientist, DSP Process Engineer - Tech Transfer and Production Support

    • Location: Vitry-Sur-Seine
    • Remote Work: 40% remote working and 10% travel expected
    • Job Type: Permanent

    About the job


    As Senior Scientist, DSP Process Engineer within our BioProcess Engineering (BPE) team, you'll lead technical transfer activities and provide critical production support for biologics manufacturing across our global network. Ready to get started?

    The BioProcess Engineering (BPE) team, part of the Mammalian Platform unit of the Global CMC Development organization, is responsible for the execution of pilot-scale batch manufacturing and technical transfers for all levels of clinical development. For early-phase clinical material production, BPE acts as receiving site coordinator on behalf of our manufacturing facilities. For late-stage clinical, early-stage commercial, and external clinical material production, BPE acts as the sending site coordinator and works closely with process owners, sourcing partners, and the Manufacturing & Supply organization.

    About Sanofi


    We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

    Main responsibilities

    • Lead technical transfer activities including facility-fit assessment and operational readiness assessment and provide technical support as SME (Subject Matter Expert) for processes (mainly DownStream Process)
    • Support GMP manufacturing operations and act as Drug Substance lead for programs from Cycle 1 to Cycle 3 when necessary
    • Partner with all relevant functions from R&D and Manufacturing & Supply to perform facility fit assessment, GMP operational readiness assessment, and authorize transfer documents
    • Act as a data steward by gathering and compiling process data for projects with support from Development, GMP manufacturing, and Analytics teams for development runs, scale-up batches, and GMP batches
    • Create data visualizations for reviews, assessments, and process anomaly root cause analysis
    • Lead evaluation and implementation of new process platforms and manufacturing technologies
    • Write and revise protocols, procedures, reports and other process-related documentation to support process scale-up, transfer, and implementation to cGMP manufacturing operations

    About you


    Skills that you have (mandatory)

    • Engineering Degree in Chemical Engineering, Biochemistry, Biotechnology, or related field with industrial experience in manufacturing or process development of biologics
    • Experience in leading matrix teams
    • Excellent oral and written communication skills to build relationships both inside and outside the company
    • Experience working on multiple complex projects to aggressive timelines with the ability to adapt to rapid changes in project priorities
    • Fluent in English, French speaking in writing, reading and presenting

    Skills that you could improve in this new position (to develop)

    • Experience in manufacturing or process development of biologics, preferably produced in recombinant protein purification systems, with knowledge on scale-up, process transfer, and cGMP manufacturing operation
    • Working knowledge in recombinant protein GMP quality standards and regulatory requirementsExperience in defining process control strategy and process validation and performing risk assessment following the QbD principle
    • Experience in Data Analysis using existing tools and willingness to develop/evaluate new ones in the context of the global Digitalization strategy

    Skills that you could offer in addition (nice to have)

    • Ability to gown and work in manufacturing areas
    • Ability to work flexible hours
    • End-to-end biologics process knowledge, including cell culture and formulation knowledge

    Why choose us?

    • Shape the future of medicine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply
    • Power industry-leading performance by leveraging digital, data, and AI-driven innovation – at speed and scale
    • Transform lives worldwide by delivering life‑changing treatments anywhere, anytime
    • Work with AI, robotics, and next‑gen automation to redefine global manufacturing and supply
    • Develop new skills, explore cross‑functional roles, and work in an environment that values growth and discovery
    • Be part of an organization that invests in people, technology, and sustainability, leading the industry in low‑carbon manufacturing and digital transformation
    • Enjoy outstanding benefits, including flexible working options, comprehensive healthcare, and well‑being programs designed to help you thrive

    Pursue Progress. Discover Extraordinary

    Join Sanofi and step into a new era of science – where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never‑been‑done‑before . You'll help push boundaries, challenge convention , and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary – together.

    At Sanofi, we provide equal opportunities to all regardless of race, color , ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

    #LI-FRA

    #LI-Hybrid

    Pursue progress, discover extraordinary

    Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.

    At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

    Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at


    #J-18808-Ljbffr

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