Quality Control Biochem / Chemistry Testing L1-1
Verna, 印度 Regular 发布于 Oct. 09, 2026 申请截止于 Nov. 09, 2026Job Title: Quality Control Biochem / Chemistry Testing L1-1
Location: Goa Site, Verna Industrial Estate, Salcete, Goa, India
About the job
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.
Sampling & Analysis
- Sampling of Raw Material, intermediate and as per the relevant SOP’s
- Ensuring proper storage as per Storage conditions for Raw Material, intermediate, stability samples and Finish Product as per the relevant SOP’s
- Handling and confirming external testing of Raw material samples.
- Management of samples in sample cabinet as per Storage conditions for Raw Material, intermediate, stability samples and Finish Product as per the relevant SOP’s
- Analysis of Raw Materials, stability samples, finished goods as per the required specifications on time.
- Ensure cGLP in the laboratory activities.
- Carry out instrumental analysis of stability samples, Raw materials, Finished Goods such as HPLC, GC, Dissolution, potentiometer, IR spectrophotometer, Raman Analyzer, Dissolution tester, Disintegration tester, Viscometer, Tap density apparatus, Microscope, UV-Vis Spectrophotometer, Conductivity meter, pH Meter, Sieve shaker, Melting point etc.
- Ensuring audit readiness in Quality control laboratory.
Documentation
- Prepare and maintain raw data and analytical records in compliance with the current regulatory requirements.
- Maintain the raw data as per regulatory requirements.
- Scanning and Proper Storage of Raw Material ATR in documentation store.
- Filling and documentation of ILI/Deviations at site.
- Review of logbooks, Calibration records, Qualification documents etc.
- Review and revise the specifications and test procedures based on the pharmacopeia.
- Raising deviations and implementation of CAPAs through Qualipso
- Carry out result recording, Review of data, printing of ATRs, Sampling instruction transactions in SAP ATHENA
- Perform qualification of new instruments.
- To support in Simplification and digitalization of activities in Quality control laboratory.
- To support in OOS/OOT and deviations related to Quality control.
Qualification/Calibration/Validation
- Carry out the calibrations and preventive maintenance of instruments as per SOP and maintain records.
- Perform qualification of instruments
- Carry out the validation of analytical methods as per the testing procedure
- Supporting in chromatographic trouble shooting
*HSE
- Adherence to all health safety & environmental aspects as required by company policies and procedures.
- Ensure that the implementation of HSE systems, safe working conditions and maintain a culture of continuous improvement.
- Conducting daily training in the +QDCI meeting address any unsafe condition.
- Take suggestion from associates to improve the work conditions with great safety and zero risk.
- Periodic review of the implemented procedures and evaluation of the same.
- Train people on safety and their job to ensure zero LTI and IWLT at workplace.
- Carry out activities related to HSE applicable to the laboratories at side
- Support the team to comply with requirements of ISO 14001 standards with respect to laboratories.
- Ensure HSE compliance in the laboratory at all times
About you
- Experience: 3 Years
- Technical skills: Raw material testing, Finished product testing, handling of instruments,basic knowledge of HPLC.
- Qualification: MSc Chemistry
- Languages: English, Hindi, Marathi
Why choose us?
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- Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
- Power industry-leading performance by leveraging digital, data, and AI-driven innovation at speed and scale.
- 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.
- Work with AI, robotics, and next-gen automation to redefine global manufacturing and supply.
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。
体验可能性
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Ama
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Cambridge Crossing
We're bringing together 2,500 people from across our organization — R&D, Medical, Commercial and Global colleagues all working to realize the power of collaboration.
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Innovation in Action
Our flexible lab of the future will transform how we conduct research, while our innovation center will be fully integrated with existing R&D locations.
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Sanofi’s AI Centre of Excellence in Toronto
The Centre is focused on using leading technologies to develop world-class data and artificial intelligence (AI) products to create value for the health sector.
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Sanofi Canada's Philanthropic Efforts
By chasing the miracles of science to improve people’s lives, we surprise ourselves with what we can achieve. Our team is humbled by the impact our efforts make.
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Sustainable and Green
Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.
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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。