Perform analysis of RM, finished, and stability samples. Handle HPLC, UPLC, GC, UV, IR, and Dissolution instruments. Maintain GMP, GLP, and ALCOA documentation practices.
Looking for enthusiastic fresher candidates for production activities in the Manufacturing Department, who are eager to start and grow their career in the pharmaceutical industry.
Candidates must have good analytical skills for testing Finished Goods of different dosage form like Tablets, Capsules, Oral Suspension, Injectables and External preparation
Analysis and processing of In process and Finished product and handling of HPLC, UV, FTIR, K/F, AAS, IC, Dissolution. Analysis of Raw material and Excipients and handling of HPLC.
Responsible for coordination with various departments like Regulatory Affairs, Manufacturing, Warehouse, Quality Assurance, Quality Control, Engineering for execution of Scale-up and Exhibit batches and reviewing GMP related documents.
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.
Looking for candidates with relevant experience in Regulatory Affairs
Post : Sr. Manager / Manager - Strategic International Expansion – RA
To perform all associate activities like reagent preparation, volumetric solution preparation, test solution preparation, factor determination, working standard preparation required for analysis as per approved procedure.