Develop and optimize new dissolution method (Biorelevant and discriminatory dissolution method) mimicking the physiological system
Independently perform and document solubility experiments, dissolution method activities and other characterization methods (DT, solubility, IDR, Viscosity etc).
Testing of various developmental formulations in biorelevant and discriminatory dissolution methods
Analysis of samples using various analytical techniques like HPLC/UPLC and spectrophotometric methods. Addressing the trouble shoots in chromatographic methods
Write protocols, reports or lab procedures based on templates under expert\'s supervision.
Document Risk assessment at pre-evaluation stage under expert\'s guidance.
Knowledge of PBPK/IVIVC models.
Assist modeling expert in developing various in-silico tools like Gastroplus/Phoenix WinNonlin etc.
Work in close collaboration with multifunctional project team
Minimum requirements
Experience of 2-4 years in Analytical development from generic pharmaceutical industry.
M Pharm (Pharmaceutical Analysis, Pharmaceutics); M Sc (Analytical Chemistry); B Pharm
Attributes required of the job e.g. the ability to work independently; the ability to work in a team; shows initiative; able to work with all levels of staff.
Strong written and oral communication skills.
Functional Area
Research & Development
Division
SANDOZ
Business Unit
Small Molecules STO
Employment Type
Regular
Commitment to Diversity & Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.