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Title:
Executive - Analytical Development
Company:
Sun Pharmaceutical Industries Ltd
- To work as per cGMP and ensure its compliance as per current guideline and SOPs.
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- Responsible to take training before execution of allotted work & maintaining the training file.
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- Responsible to follow safety precaution as per laboratory procedure.
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- Responsible to escalate any issue / incident to reporting manager for prompt corrective action.
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- Responsible for method development studies for various finished products.
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- Responsible for method Validation studies for various finished products.
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- Responsible for routine and stability studies of various finished products.
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- Responsible to align with organization goal.
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- Other responsibilities assigned by reporting authority.
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- Responsible to follow Quality Management Document procedure.
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- Responsible to perform the calibration of instrument.
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- Responsible to prepare Study Protocol and Study Reports.
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- Responsible to maintain instrument/equipment as per SOPs.
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- Responsible for timely archival of documents as per SOP.
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- Responsible to follow safety precaution as per laboratory procedure.
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- Responsible to ensure proper Handling and Disposal of waste.
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