Compliance Lead
沃特福德, 爱尔兰 Fixed Term (Fixed Term) 发布于 Aug. 19, 2026 申请截止于 Aug. 27, 2026 Salary Range EUR 54,800.00 - 73,066.66Job Title: Manufacturing Compliance Lead
Location: Waterford, Ireland
About the job
As a Compliance Leader, you play a critical operational leadership role within Lyo Operations, ensuring the compliance in the department at Sanofi is effectively maintained and enhanced.
You are accountable for cGMP & HSE compliance, training, and maintaining inspection readiness for complex aseptic systems for sterile vial filling and Lyophilisation area.
You act as the central coordination point across all functions involved for compliance. While you are not directly accountable for the performance of other departments, you are responsible for establishing and maintaining the governance framework that enables each function to meet its commitments. This includes identifying performance gaps, escalating risks, and driving corrective actions where required.
Ready to get started?
Join a global network that powers how Sanofi delivers - seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.
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:
- Raising and management of all Quality System processes including Change Controls, Deviations, Tasks, Quality Events etc.
- Driving of all Quality Metrics for the department
- Forward review of Quality Metrics to ensure no over-dues
- Procedure effectiveness and simplification and actively contribute to continuous improvement initiative
- Ensure Training is fit for purpose and complies with all applicable legislative requirements.
- Ensure effective co-ordination and support for external and internal audits for the department.
- Perform critical / constructive review of procedures and practices.
- Identify and lead projects to make step change improvements to the departments Quality.
- Conduct duties in a safe manner and report all safety issues or concerns
- Support leadership team in achieving goals / tasks
- Attend offline department meetings and be the voice of the department.
- Actively contribute to continuous improvement initiatives utilising lean methodologies where appropriate.
- Liaise with Quality Representative to support and improve RFT in the area and Always Audit Ready.
- Complete all duties as per relevant SOPs
- Ensure compliance to cGMP at all times
About you
Degree in Life Sciences, Engineering, Pharmacy, or a related discipline
Minimum of 3 years’ experience in a similar or related role
Significant experience in a biopharmaceutical or pharmaceutical manufacturing environment.
Demonstrated experience in cross-functional coordination
Extensive knowledge of cGMP and GDP in a regulated environment
Specialist knowledge of training and quality systems in a regulated environment
Excellent accuracy and attention to detail
Excellent interpersonal skills
Good Presentation skills
Working knowledge of MS Office
Effective personnel and project management skills
Business awareness and continuous improvement techniques
Knowledge of Lyophilisation and associated processes or biologics manufacturing processes is an advantage
Why choose us?
Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.
PursueProgress. DiscoverExtraordinary.
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.
追寻 发展。探索 菲凡。
加入赛诺菲,开启科学新时代。在这里,你的成长将如我们的工作成果一样具有变革性。我们帮助你发展,助你走得更远、思考得更快、做前所未有的事。你将与我们一起突破边界、挑战常规,打造更智慧的解决方案,惠及全球社区。准备好追寻科学的奇迹,改善人们的生活了吗?让我们携手追寻发展,探索非凡。
赛诺菲致力于为所有员工提供平等的就业机会,不因种族、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、性别认同、受保护的退伍军人身份或其他受法律保护的特征而有所差异。
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。
体验可能性
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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。