Executive - Analytical Development
SUN PHARMA
Date: 9 hours ago
City: Vadodara, Gujarat
Contract type: Full time
- 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 of API, Drug Product & In process Material preferably Peptide molecules
- Responsible for method Validation studies of API, Drug Product & In process Material preferably Peptide molecules
- Responsible for routine and stability studies of API, Drug Product & In process Material preferably Peptide molecules
- Responsible to perform the pharmacopeial evaluation study as per requirement.
- Responsible to align with organization goal.
- Other responsibilities assigned by reporting authority.
- 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.
- Responsible for timely archival of documents as per SOP.
- Responsible to follow safety precaution as per laboratory procedure.
- Responsible to ensure proper Handling and Disposal of waste.
- Responsible to qualification reference standard / working standard/chemical reference standard samples as per approved and valid procedure.
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