Quality Control Biochem / Chemistry Testing L1-1
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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 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?
.
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.
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, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1523 comparable Quality roles across 149 biopharma companies.
Salary context
248 of 1523 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1523 comparable roles
+ 47 more countries
Seniority mix
690 of 1523 peers have a known seniority level
Therapeutic area mix
1 of 1523 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.