At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
Are You Ready to Create Your Own Sunshine?
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key responsibilities:
Analysis of Finished Product samples /Process Validation samples /Stability samples/ RM. Samples /Cleaning validation samples and Beta-lactam containment monitoring samples as per SAP Request /Process Validation Protocol /Stability Protocol /and Cleaning validation protocol and STP’s.
Documentation of analytical activity performed.
Document analytical data and calculate results.
To assist in investigation of OOS /OOT/Deviation /Lab Events.
Management of Finished Product /Process Validation samples as per respective SOP’s.
Ensure integrity, accuracy and adequacy of the analysis performed.
Document data accurately and maintain neat/concise/organized Finished Product /Process Validation records.
Ensure compliance to cGMP requirements and laboratory procedures.
Preparation of RAPS (Record of analysis) of FP/PV Whenever required.
To participate in analytical method transfer and analytical method Validation activity (Like analysis, Documentation & reporting of results).
Timely Place the indents & Procurements of Laboratory chemical & Consumables.
Recording of results in SAP system.
Travel Estimate
Job Requirements
Educational Qualification
M.Sc / B.Pharm
Experience
Tenure: 2-5 years
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities We provide robust advantages and opportuni
📌 Officer-QC (API) (Dewas)
🏢 Sun Pharmaceutical Industries
📍 Dewas
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