B. Pharm , M.Sc. , M. Pharm with 2-8 years of relevant experience in IPQA , validation , Documentation related activities in Oral Solid,Oral Liquid,Semi Solid dosages manufacturing facilities.
Amneal Pharmaceuticals, Inc is a global pharmaceutical company. Our team of 7,500+ colleagues helps make healthy possible through the development, manufacturing, and distribution of a diverse portfolio of 270+ high-quality medicines. Amneal is a global essential medicines company powered by a robust U.S. generics business. Amneal is a growing branded business with deepening portfolios in institutional injectables, biosimilars and select international markets including India.
Accountable for regulatory transition activities to achieve relevant project turning points, as well as core business development operational activities including but not limited to running the green light process, preparation of documentation and risk, issue management.
Bachelors or Masters degree in Pharmacy, Pharmaceutical Sciences. Lead and manage the technology transfer of pharmaceutical formulations from R&D to manufacturing Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs
Bachelors or Masters in Pharmacy. Must have exposure in handling of Process Area maintenance like Manufacturing Vassals, Filling machine, Autoclave, Isolators and Lyophilization.
M. Pharm / M. Sc / B. Pharm / B. Sc; Experience in Method Validations and Verifications, Analytical Method Transfers with Brazil Regulatory exposure. Experience in Finished Product, In-Process, Stability and GLP activities
M.Pharm; Analytical Method Validation. Development, Transfer activities. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule