Bench Scientist - Anti-drug-Antibody-Assays with Dried Blood Spot Samples / Patient Centric Sampling (all genders)
法兰克福, 德国 Fixed Term (Fixed Term) 发布于 Apr. 23, 2026 申请截止于 May. 08, 2026 Salary Range EUR 79,104.00 - 105,472.00About 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.
About the Role
Our Team:
Sanofi's Translational Medicine Unit (TMU) Germany team is part of Sanofi's global network, among other things specializing in bioanalytical method development and immunogenicity testing. We want to rapidly implement innovative analytical solutions with external partners. Our mission is to advance patient-centric approaches in clinical testing — making sample collection more convenient for patients while maintaining the highest scientific standards. This role offers the opportunity to contribute to groundbreaking research that directly impacts how clinical trials are conducted worldwide.
Main Responsibilities:
- Establish and optimize anti-drug antibody (ADA) assay methods in the laboratory, including method transfer and setup of analytical procedures
- Research, evaluate, and select dried blood spot (DBS) collection devices for immunogenicity testing applications, considering both scientific and sustainability criteria
- Design and execute feasibility experiments comparing traditional liquid samples to DBS-derived samples, including sensitivity assessments and method comparison studies
- Develop comprehensive validation plans for new sample collection methods in accordance with regulatory guidelines and industry best practices
- Prepare detailed scientific reports and present findings to internal stakeholders and external partners for decision-making processes
- Collaborate closely with TMU to facilitate rapid implementation of validated methods with external laboratory partners
- Support technology transfer activities to enable broader adoption of patient-centric sampling approaches across multiple testing sites
About You
Education & Professional Experience
- Master's degree or PhD in biochemistry, biology, pharmaceutical sciences, or a related field
- Hands-on experience in bioanalytical method development and validation, ideally in immunogenicity or ligand-binding assays
- Experience with anti-drug antibody (ADA) assays or similar immunoassay platforms is a strong advantage
- Familiarity with GxP environments and regulatory guidance documents (e.g., EMA/FDA immunogenicity guidelines)
Social Competencies
- Strong collaborative mindset — able to work effectively across teams and functions in an international environment
- Excellent communication skills, both written and verbal, with ability to present complex scientific data to diverse audiences
- Ability to work independently and take ownership of deliverables within a defined project framework
- Openness to innovation and patient-centric approaches
Technical Skills
- Proficiency in immunoassay techniques (ELISA, ECL, or similar platforms)
- Experience with dried blood spot (DBS) technology is a plus, but not required
- Familiarity with method validation principles and SOPs, experiences in regulated bioanalysis are a plus
- Ability to document, analyze, and present scientific data clearly
Languages
- English: fluent (essential for international collaboration and external partner communication)
- German: beneficial for local operations
Pursue Progress. Discover Extraordinary.
Advancing science is our purpose. Every day. Always. But progress doesn't happen without people — people with different backgrounds, in different places, in different functions, all united by one thing: the desire to work miracles.
At Sanofi, we are committed to equal opportunities for all, regardless of age, ethnic origin and nationality, gender and gender identity, physical and mental abilities, religion and beliefs, sexual orientation, social background, or family status.
Learn more about our programs for diversity, equity, and an inclusive work environment in our ALL IN video and at www.sanofi.de.
Join our great team!
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!
最终薪酬将根据已展现的经验、技能、工作地点和其他相关因素确定。员工可能有资格参与公司员工福利计划。
请注意,对于德国的关税职位,薪酬基于化学工业联邦集体谈判协议核定。
体验可能性
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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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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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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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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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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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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。