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Hiring alert!
Sun Pharmaceutical Ltd
Opening in MS&T Orals
Job Location: Halol, Gujarat
Experience: 3-7 years
Qualification: M.Pharm
Job Description :
1) The person will be Responsible for driving below activities of MS&T.
Exhibit Projects, New Launch Projects and Troubleshooting Projects
2) To coordinate with different departments i.e. Formulation Development, Production, Engineering, Quality Control, Quality Assurance, Packaging and any other for the timely execution of the projects.
3) To keep the track / plan & monitor for the Trial, Scale up and Exhibit & Pre PV/PV Batches.
4) To review / approve documentation i.e. trial batch objective, trial batch BMR, protocol, report, justification / technical report / regulatory query response / write up for any recommendation / data compilation / study protocol / report etc.
5) To attend / plan meetings for moving forward the projects.
6) To assist the CFT (Production / QA / QC etc department) for resolving the Trouble shooting Projects, Trial / Scale Up Batches manufacturing / EB / CH / PV Batches manufacturing.
9) To initiate/review/ evaluate Investigations, Change Control, CAPA, Deviation or any other QMS related documents in Trackwise® System.
Send your resume on: Hr.tandalja@sunpharma.com
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Interview Data Loading …
Hiring alert!
Sun Pharmaceutical Ltd
Opening in MS&T Orals
Job Location: Halol, Gujarat
Experience: 3-7 years
Qualification: M.Pharm
Job Description :
1) The person will be Responsible for driving below activities of MS&T.
Exhibit Projects, New Launch Projects and Troubleshooting Projects
2) To coordinate with different departments i.e. Formulation Development, Production, Engineering, Quality Control, Quality Assurance, Packaging and any other for the timely execution of the projects.
3) To keep the track / plan & monitor for the Trial, Scale up and Exhibit & Pre PV/PV Batches.
4) To review / approve documentation i.e. trial batch objective, trial batch BMR, protocol, report, justification / technical report / regulatory query response / write up for any recommendation / data compilation / study protocol / report etc.
5) To attend / plan meetings for moving forward the projects.
6) To assist the CFT (Production / QA / QC etc department) for resolving the Trouble shooting Projects, Trial / Scale Up Batches manufacturing / EB / CH / PV Batches manufacturing.
9) To initiate/review/ evaluate Investigations, Change Control, CAPA, Deviation or any other QMS related documents in Trackwise® System.
Send your resume on: Hr.tandalja@sunpharma.com
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