1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.00 LPA
Job responsibilities:Preparation, Compilation and review of registration dossier of tablet /capsule/injection in CTD,ACTD as well as country specific format for countriesPreparation, Compilation and review of registration dossier of capsule/syrup/balm in a Herbalproducts for country specific format in countries of African Region, Cambodia, Myanmar, CISTo manage new registration / preregistration / ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 8.00 LPA
Provide leadership planning and work assignment.
Drug licence application and renewable of licence in State Drug Authority for different type of Formulation.
Monitoring & Maintaining Quality Systems in the plant to meet State GMP requirements.
To organize inspection & testing of Raw Material, In-Process & Finished Products.
Planning and carrying out self-inspection of all ...