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Senior Scientist DP Development

Marcy-l'Étoile, 法国 Permanent Posted on   Jan. 07, 2025 Closing on   May. 07, 2025
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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 DP Development

About the job

In the race for the future of health – The Sanofi mRNA Center of Excellence (CoE)

At Sanofi, we chase the miracles of science, and we know mRNA has a role to play in the future of health. And while the pandemic has shaken up our industry, creating new opportunities and risks, we believe the acceleration of innovation with mRNA technology means vaccines and treatments for more people faster than before.

That’s why we’re looking for bold, optimistic world-changers to join our mRNA Center of Excellence. We’re investing €400m a year into the new Center, hiring a team of 450 dedicated employees, and focusing on implementing an integrated end-to-end mRNA vaccine capabilities and research with R&D, digital and CMC teams.

Bring your ambition and optimism and join us on our journey to discover and deliver transformative medicine to patients through the advancement of our cutting-edge mRNA technology!

Our Team

The mRNA – Senior Scientist Drug Product Development is part of the Global Drug Product Development (GDPD) group within the mRNA CoE. GDPD is responsible for developing the Drug Product formulation and manufacturing process in support of all ongoing mRNA Vaccine programs within the CoE from Phase 1 through Phase 3 and commercialization. GDPD achieves this through internal collaborations with ourcolleagues in US and through constant collaboration with other departments including Drug SubstanceDevelopment, Analytical Sciences, Research, Process Industrialization, Global ProcessHarmonization & Tech Transfer, and cGMP Strategic Supply & Operations. GDPD’s mission is to developsafe, stable, and patient-centric mRNA vaccine and therapeutic Drug Products and associated robustmanufacturing processes.

Main responsibilities:

  • Apply scientific expertise and judgment to initiate, design and execute orsupervise executionof the development of liquid and lyophilized mRNA-LNP drug productformulation and process
  • Make scientific presentations and report project progress within mRNA CoE Formulation teams and with partners and in international forums
  • As a Subject Matter Expert in drug product development, be an impactful contributor to project teams and actively participatein DP sub-teams
  • Provide consolidated DP development technical work packages with timelines, resources and critical path activities
  • Drive organizational goal of rapidly incorporating innovative advances in drug product platform (thermostable formulations and process improvements)
  • Promote innovation, state of the art technologies, and propose strategies using publications to improve the products
  • Proactively collaborate with other functions to meet projects and platform milestones
  • Proactively collaborate with other groups or sites in transfer of information, materials anddrugproduct technology
  • Promote internal assessment of new DP technologies and scientific network to leverage internal and external expertise
  • Make decisions that require developing new options to solve moderately complex problems
  • Demonstrate continuous growth in depth and breadth of personal scientific knowledge andunderstanding of strategic goals of group, team, and company
  • Maintain a consistent record of publications, patents, external presentations
  • Proactively participate in laboratory organization(including HSE, quality aspects) and continuous improvement of WoW
  • Supervise lab activities with technicians, internships and TPW (indirect report), when appropriate

About your development opportunities

In this role, you will gain a technical understanding of mRNA vaccine drug product development, drug product characterization techniques, and process development study design strategies. You will be exposed to, and gain an understanding of, what other technical function are responsible for and how they all play a role in mRNA vaccine development. You will have the opportunity to collaborate and learn from management within GDPD as well as other departments.

About you

  • Experience: Experience in CMC activities and project management, parenteral drug product development and industrialization required. Understanding of complex R&D landscapes globally, ability to identify cutting-edge technologies and new directions, strong academic and biotech/pharma scientific networks
  • Soft skills: Good oral communication, proactive, organized, passionate about scientific progression, leadership, and interpersonal skills. Ability to work in a fast-paced environment
  • Technical skills: Formulation, Physical-chemistry of nanoparticles and associated characterization methods, pharmaceutical engineering, knowledge on different unit operations of drug product manufacturing (Lipid Nanoparticles manufacturing, TFF, Freeze/Thaw, mixing, filtration, Fill&Finish, lyophilization), process modelization, digital tools
  • Education: Biochemistry, chemistry, pharmaceutical engineering or related degree, PhD
  • Languages: French & English

PursueProgress.DiscoverExtraordinary.

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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s 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, or gender identity.

Watch ourALL IN videoand check out our Diversity Equity and Inclusion actions atsanofi.com!

#LI-FRA

#mRNA

追寻 发展探索 菲凡

进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。

在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。

观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!

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在法国的职位

我们在法国拥有20,000名员工,分布在28处办公地点。他们肩负着相同的使命:将药物和疫苗带给最需要的人。从入职第一天起,您就能参与重要项目,找到职业发展的航向。无论您是研究员还是市场营销人员,我们都将为您提供相应的工具、资源和支持,帮助您不断追求进步。发展您的个人能力,携手具有包容性的团队,一起改变全球数百万人的生活。

体验可能性

  • 我们的办公地点

    我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。

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  • 勇敢追梦,奔赴美好未来

    想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。

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  • 您和我们相互依存,共同成长

    我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。

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  • 心怀梦想,成就一番事业

    我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。

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  • Ama

    Ama puts her project management techniques and ServiceNow knowledge to use to help advance Sanofi’s Digital Data operating model. Learn how our team connects data and AI to do what’s never been done before.

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  • Cambridge Crossing

    We're bringing together 2,500 people from across our organization — R&D, Medical, Commercial and Global colleagues all working to realize the power of collaboration.

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  • Innovation in Action

    Our flexible lab of the future will transform how we conduct research, while our innovation center will be fully integrated with existing R&D locations.

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  • Sanofi’s AI Centre of Excellence in Toronto

    The Centre is focused on using leading technologies to develop world-class data and artificial intelligence (AI) products to create value for the health sector.

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  • Sanofi Canada's Philanthropic Efforts

    By chasing the miracles of science to improve people’s lives, we surprise ourselves with what we can achieve. Our team is humbled by the impact our efforts make.

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  • Sustainable and Green

    Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.

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  • 我们的人与文化

    我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。

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  • 我们的故事

    我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。

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  • 为什么选择我们?

    我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。

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