Novartis Pharmaceuticals Employee Reviews for Associate Scientist

"I learned a lot of new things and understood how corporates work."

What do you like about working at Novartis Pharmaceuticals?

"I loved the corporate culture. I was acknowledged as an independent employee and my opinions and style of work was appreciated."

Do you have any tips for others interviewing with this company?

"Do homework, know about the company and current projects. Your sincerity towards work counts the most."

What don't you like about working at Novartis Pharmaceuticals?

"Being a big corporation my duties were limited to selective profile, I did not get to explore different areas."

What suggestions do you have for management?

"Did not get much opportunity to work with the management."

What do you like about working at Novartis Pharmaceuticals?

"Formulation Scientist. 2006-Present Novartis Pharmaceutical Corporation, Associate Scientist (Formulation Development) Broad experience in developing formulation and optimization of various dosage forms, IR, CR and coating from early development to late stage projects (Phase I to Phase III)Experienced in solid oral dosage forms including tablets (Bilayer and Multilayer) and capsulesDesigned and executed various project using appropriate technologies for Clinical studies, Optimization and Scale-upExtensive hands on training with direct compression, dry granulation (Roller Compaction and Melt Extrusion), capsulation and wet granulation (High and Low Shear), compression (Bilayer Tablet Press) and coatingExtensive hands on experience with dissolution and HPLC analysisPlanned and executed sequential experimental strategies to evaluate multiple parameters, including excipients and processing methodsFormulated and manufactured Clinical supplies for several New Chemical Entities in early phase studiesCharacterized Physical/Chemical properties of various APIsExtensive experience in writing Batch Records, Manufacturing Instructions, Technology Transfer reports for Pilot and Prevalidation batches and supported with NDA submissions reports/presentations.Experience with supervising lab/clinical manufacturing techniciansGeneral pharmaceutical knowledge on FDA, USP, HPFBI, GMP, cGMP, GLP, GCP, ICH guidelines, and in writing and reviewing protocols, SOPs and other technical documentations including Validation reviews."

Do you have any tips for others interviewing with this company?

"know your material"

What suggestions do you have for management?

"good"