Quality Control Analyst
沃特福德, 爱尔兰 Fixed Term (Fixed Term) 发布于 Jul. 28, 2026 申请截止于 Aug. 17, 2026 Salary Range EUR 48,000.00 - 64,000.00Quality Control Analyst
Location: Waterford, Ireland
Job Type: 23-month FTC
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About the job
Our Team
Quality Control (QC) is responsible for sample receipt, testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation.
The Quality Control Operations group supports Laboratory Investigations, Deviation Investigations, CAPA support, Training, and Change Controls. Quality Control Validation Support consists of the Method Validation Group and the Equipment Qualification Group. Quality Control is also responsible for assisting in site-wide studies and projects.
Main Responsibilities
• Execute analytical testing in a timely manner, ensuring adherence to committed scheduled plans
• Perform tasks in accordance with cGMP and HSE requirements, following all associated instructions, procedures, and records
• Record all expected raw data, calculations, and information to comply with cGMP and data integrity requirements
• Ensure appropriate training and qualification for assigned analytical testing
• Perform QC data review of tests executed by other analysts in a timely manner
• Inform management of any quality or HSE events (deviations, out-of-specification results) promptly to ensure proper investigation and impact assessment
• Participate actively in investigations to ensure thorough analysis and appropriate impact assessment
• Execute assigned CAPAs related to remediation plans and continuous improvements
• Maintain laboratory facilities and instruments in quality and safety status to ensure appropriate use
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About you
• Education: BSc in Chemistry, Biochemistry, or a related science discipline
• Experience: Background in an analytical chemistry laboratory environment
• Technical skills:
• Knowledge of cGMP and laboratory safety requirements
• Analytical testing and data review capabilities
• Understanding of data integrity principles
• Experience with Biologics and/or HPLC/UPLC, CE, ICE techniques
• Soft skills:
• Attention to detail and accuracy in documentation
• Strong communication skills for reporting and collaboration
• Problem-solving abilities for investigations
• Commitment to quality and safety standards
• Team collaboration and active participation
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Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But 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. So, let's be those people.
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 our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
#LI-EUR
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。
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