At Sun Pharma, we commit to helping you Create your own sunshine— by fostering an setting 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
📌 Officer-QC (API) (Dewas)
🏢 SUN PHARMA
📍 Dewas
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