Quality Control Biochem / Chemistry Testing L1-1

Sanofi; India; On-site; INR 520,000 - 820,000; Full time

Job summary

Sanofi Goa site is seeking a QC Biochemist / Chemistry Testing L1-1 to join its Sampling & Analysis team. You will handle raw material, in-process, and finished product testing, follow SOPs, maintain proper documentation, and ensure GLP in the laboratory.

The role requires MSc in Chemistry, 3 years of hands-on experience in QC labs, and proficiency in English, Hindi, and Marathi. You will work with HPLC, GC, dissolution and other instruments, contributing to audit readiness and continuous

Qualifications

• 3 years of experience in quality control or related field.
• MSc Chemistry or equivalent qualification.
• Proficiency in English, Hindi and Marathi.

Responsibilities

• Sampling of Raw Material, intermediates and finished products per SOPs.
• Instrumental analysis using HPLC/GC/Dissolution per specs.
• Ensure GLP/audit readiness in QC laboratory.
• Maintain raw data, calibration records and documentation.

Skills

Raw material testing

Finished product testing

Handling of instruments

Basic knowledge of HPLC

Education

MSc Chemistry

Tools

HPLC

GC

Dissolution

IR spectrophotometer

Raman

Viscometer

pH meter

Job description

Job 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 asper Storage conditions for Raw Material,intermediate, stability samples and FinishProduct 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 ofactivities in Quality control laboratory.
• To support in OOS/OOT and deviations relatedto 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?

.

• 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.