At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an workplace 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.”
Job Description:
To work as per cGMP and ensure its compliance as per current guideline and SOPs.
Responsible to take training before execution of allotted work & maintaining the training file.
Responsible to follow safety precaution as per laboratory procedure.
Responsible to escalate any issue / incident to reporting manager for prompt corrective action
Responsible for method development studies for various finished products.
Responsible for method Validation studies for various finished products.
Responsible for routine and stability studies of various finished products
Responsible to follow Quality Management Document procedure.
Responsible to perform the calibration of instrument.
Responsible to prepare Study Protocol and Study Reports.
Responsible to maintain instrument/equipment as per SOPs.
Travel Estimate
NA
Job Requirements
Educational Qualification
Qualification: M.Pharm/M.Sc
Experience
Tenure 2-5 years of relevant experience in handling Non Orals dosage forms.
Your Success Matters to Us
At Sun Pharma, your success and well-being are our top priorities We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together
Disclaimer: T
📌 Executive -Analytical Development (Vadodara)
🏢 Sun Pharmaceutical Industries
📍 Vadodara
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