Regulatory Site Officer - all genders - Fixed-term contract until 26.02.2027
法兰克福, 德国Sas van Gent Wijk, 比利时 Fixed Term 发布于 Dec. 03, 2025 申请截止于 Dec. 18, 2025
About the job
External Manufacturing and Supply Large Molecule Specialty Care (EM&S LM SC) is responsible for GxP oversight of Contract Manufacturing Organizations (CMOs), Contract Laboratory Operations (CLOs), Distribution Centers and business partners involved in the manufacture, testing, storage and transport of Sanofi products. EM&S LM SC staff interact with functional units within other Sanofi sites, and other organizations within the External Manufacturing and Supply and Specialty Care network (e.g. procurement, supply chain, finance) to ensure compliance with internal and regulatory requirements, and to disposition intermediates (e.g. API, drug substance) and finished products with minimal risk to quality or product supply.
EM&S LM SC has responsibility for CMO and CLO and distribution activities related to products treating Rare Diseases and Rare Blood Disorders, Multiple Sclerosis (MS), and Oncology.
EM&S LM SC has offices based in Northborough and Cambridge, MA US; Frankfurt Germany; Ghent and Geel, Belgium and Amsterdam, the Netherlands
Main responsibilities:
This function can also support to other EM&S entities than EM&S LM SC.
Acts as a local regulatory interface between the external and internal manufacturing sites, quality units, MSAT, Global Regulatory Affairs and Sanofi affiliates
Collaborates closely with EM&S LM SC personnel in order to ensure compliant manufacturing and release operations
Manages and reviews CMC (Chemistry, Manufacturing and Controls) dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility
Reviews and approves cGMP or regulatory reports / change controls / protocols/ submissions and associated action plans in order to ensure regulatory and cGMP compliance
Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details
Acts as a source of regulatory expertise for others and gives advice on own area to other functions and employees
Supports and ensures GMP and regulatory compliance and inspection readiness for products under ownership of EM&S LM SC
Supports dossier Compliance program in compliance to Sanofi Global Procedures.
Support for Deviation and CAPA
Additional Responsibilities
Support the Qualified Person in any GMP and regulatory aspects related to batch release of product, as applicable
May support internal regulatory assessment of information to support internal or external audits and supplier qualification as required
Support CMO compliance via GxP and regulatory documentation review and on-site visits/Person in Plant/audits if applicable.
Frequent inter-departmental, inter-organizational and external interactions
Support the development and management of quality agreements between Sanofi and the contractor
Support program for maintaining performance metrics
About you
Education
Bachelor’s degree with scientific background or equivalent and 5+ years of experience in a GxP or regulatory affairs environment. OR
Master’s degree with scientific background and 3 years of experience in a GxP or regulatory affairs environment
Experience
A working knowledge of conventional and biotechnological and small molecule manufacturing operations, aseptic processing, validation principles, quality control techniques and testing methodologies of drug substances and drug products is beneficial.
Experience within EM&S environment and/or as regulatory compliance responsible is an asset.
Knowledge and experience with regulatory database system (Veeva RIM) is an asset.
Soft and technical skills:
Good understanding of quality and regulatory systems and management tools.
Knowledge and experience of EU/US GMPs for the biotech/pharmaceutical industry, with an understanding of worldwide regulatory affairs.
Demonstrated ability to perform work that consistently requires independent decision making and the exercise of independent judgment and discretion.
Problem solving and technical writing skills.
Ability to multitask effectively
Willingness to travel
Languages: Good written and verbal communication in English
Why choose us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Benefit from a well-thought-out benefits package that rewards your contribution and commitment.
PursueProgress. 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. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
PursueProgress. 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. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
null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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我们的产品设计师负责帮助人们提高免疫力,物流专家负责将药物送到需要的人手中,而数据分析师则借助先进的技术改善人们的生活。在医疗健康领域,每一次进步都离不开所有人的努力。您可以自由选择自己的职业发展道路。Gig零工项目将帮助您尝试更多岗位,个性化指导将为您挖掘自己从未被发现的优势。加入我们,开启菲凡的职业发展之路。您到底可以走多远?让我们拭目以待!
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勇敢追梦,奔赴美好未来
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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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我们的人与文化
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我们的故事
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