Data Integrity Expert
新加坡, 新加坡 Permanent 发布于 Nov. 19, 2025 申请截止于 Dec. 31, 2025About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
Sanofi Manufacturing and Supply organization is preparing its future through an ambitious program named Modulus Facility. The Modulus Project is at the cornerstone of Sanofi strategy as it aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable and agile, leveraging new disruptive technologies, to better address vaccine business challenges as well as Specialty Care Biologics products. One of these two Modulus facilities is constructed in Tuas (Singapore) at a new Greenfield site, with a design identical to the one in Neuville (France). The facilities will also have highly digitalized and automated capabilities which is a key enabler for operations using technologies such as autonomous guided vehicles (AGVs), cobots and cloud systems.
As Data Integrity Expert, you are to work closely with the respective Tuas functional teams to provide oversight and guidance for data integrity and projects related to data integrity to achieve the site’s digital ambition while in compliance with data integrity requirements. In addition, this role will lead the site self-inspection program to ensure the key compliance principles are embedded in the site processes and practices. He/she will also lead the site Quality Culture program, enabling the right Quality Culture to be embedded.
Main Accountabilities:
Ensuring compliance with regulatory requirements and company policies related to data integrity
Conducting regular routine data quality checks and validations to identify and address any data integrity issue
Developing and delivering training programs on data integrity principles and practices
Identifying and assessing risks related to data integrity and implementing mitigation strategies
Ensuring proper documentation practices are followed, including data recording, storage, and retrieval
Investigating data integrity incidents, including potential data breaches or falsification incidents, and implementing corrective and preventive actions (CAPA)
Leading continuous improvement initiatives to enhance data integrity practices
Overseeing the validation of computerized systems to ensure they meet data integrity requirements
Ensuring inspection readiness and participating in regulatory inspections and audits related to data integrity
Generating and reviewing data integrity reports and metrics for management, especially the DIMM (DI Maturity Model)
Representing the site in the CoP led by global and, if requested, participating in the CoE and ensuring local communication
Establish and prioritize data integrity objectives for the site
Proactively identify remediation actions from findings from internal and external audits
Identify training needs and content for data integrity
Decide on corrective and preventive actions for data integrity issues
Advise on cross-departmental data integrity strategies
About You
Education:
Bachelor’s or Master’s degree in Pharmacy, Science, Engineering, or related Life Sciences or Technology fields.
Expected Experience:
A minimum 7-10 years of relevant experience in the pharmaceutical or biotechnology industry.
5 years of experience in ensuring compliance with regulatory requirements related to data integrity in the pharmaceutical industry.
Expected Technical Skills:
Ability to analyze complex data sets and identify patterns, discrepancies, and areas for improvement
High level of accuracy and attention to detail in data recording, auditing, and reporting
Strong verbal and written communication skills to effectively train staff, report findings, and collaborate with various departments
Proficiency in identifying root causes of data integrity issues and developing effective corrective and preventive actions
Expertise in using and validating computerized systems and software relevant to data integrity management
Soft Skills:
Driven team player with the ability to collaborate and work with cross-functional teams (including global partners) to meet project timelines.
Good communication skills to present strategies to the site management and other functions.
Familiar with Digital 4.0 concepts and potential applications in Quality.
Able to work independently with little supervision.
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!
体验可能性
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Sustainable and Green
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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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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
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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。