
Scientist
1 week ago
Major Accountabilities
- 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
**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._
**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.
**Division**
SANDOZ
**Business Unit**
Small Molecules STO
**Country**
India
**Work Location**
Hyderabad, AP
**Company/Legal Entity**
Sdz Pvt Ind
**Functional Area**
Research & Development
**Job Type**
Full Time
**Employment Type**
Regular
**Shift Work**
No
**Early Talent**
No
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